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MedKoo Cat#: 535131 | Name: Formparanate

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Formparanate is a bioactive chemical.

Chemical Structure

Formparanate
Formparanate
CAS#17702-57-7

Theoretical Analysis

MedKoo Cat#: 535131

Name: Formparanate

CAS#: 17702-57-7

Chemical Formula: C12H17N3O2

Exact Mass: 235.1321

Molecular Weight: 235.29

Elemental Analysis: C, 61.26; H, 7.28; N, 17.86; O, 13.60

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
Formparanate
IUPAC/Chemical Name
Carbamic acid, methyl-, ester with N'-(4-hydroxy-o-tolyl)-N,N-dimethylformamidine (8CI)
InChi Key
NPCUJHYOBSHUJJ-RIYZIHGNSA-N
InChi Code
InChI=1S/C12H17N3O2/c1-9-7-10(17-12(16)13-2)5-6-11(9)14-8-15(3)4/h5-8H,1-4H3,(H,13,16)/b14-8+
SMILES Code
CN(C)/C=N/C1=CC=C(OC(NC)=O)C=C1C
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 235.29 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Kabir E, Mu G, Momtaz DA, Bryce NA, Teets TS. Formazanate Complexes of Bis- Cyclometalated Iridium. Inorg Chem. 2019 Sep 3;58(17):11672-11683. doi: 10.1021/acs.inorgchem.9b01657. Epub 2019 Aug 20. PMID: 31430140. 2: Gilroy JB , Otten E . Formazanate coordination compounds: synthesis, reactivity, and applications. Chem Soc Rev. 2020 Jan 2;49(1):85-113. doi: 10.1039/c9cs00676a. PMID: 31802081. 3: Kabir E, Patel D, Clark K, Teets TS. Spectroscopic and Electrochemical Properties of Electronically Modified Cycloplatinated Formazanate Complexes. Inorg Chem. 2018 Sep 4;57(17):10906-10917. doi: 10.1021/acs.inorgchem.8b01543. Epub 2018 Aug 16. PMID: 30112907. 4: Mondol R, Otten E. Aluminum Complexes with Redox-Active Formazanate Ligand: Synthesis, Characterization, and Reduction Chemistry. Inorg Chem. 2019 May 6;58(9):6344-6355. doi: 10.1021/acs.inorgchem.9b00553. Epub 2019 Apr 12. PMID: 30978008; PMCID: PMC6506801. 5: Kamphuis AJ, Milocco F, Koiter L, Pescarmona PP, Otten E. Highly Selective Single-Component Formazanate Ferrate(II) Catalysts for the Conversion of CO2 into Cyclic Carbonates. ChemSusChem. 2019 Aug 8;12(15):3635-3641. doi: 10.1002/cssc.201900740. Epub 2019 Jul 9. PMID: 31038791. 6: Milocco F , Demeshko S , Meyer F , Otten E . Ferrate(ii) complexes with redox-active formazanate ligands. Dalton Trans. 2018 Jul 3;47(26):8817-8823. doi: 10.1039/c8dt01597j. PMID: 29922783. 7: Milocco F , de Vries F , Dall'Anese A , Rosar V , Zangrando E , Otten E , Milani B . Palladium alkyl complexes with a formazanate ligand: synthesis, structure and reactivity. Dalton Trans. 2018 Oct 23;47(41):14445-14451. doi: 10.1039/c8dt03130d. PMID: 30183797. 8: Dhindsa JS, Melenbacher A, Barbon SM, Stillman MJ, Gilroy JB. Altering the optoelectronic properties of boron difluoride formazanate dyes via conjugation with platinum(ii)-acetylides. Dalton Trans. 2019 Oct 10. doi: 10.1039/c9dt03417j. Epub ahead of print. PMID: 31599277. 9: Maar RR, Hoffman NA, Staroverov VN, Gilroy JB. Oxoborane Formation Turns on Formazanate-Based Photoluminescence. Chemistry. 2019 Aug 22;25(47):11015-11019. doi: 10.1002/chem.201902419. Epub 2019 Jul 8. PMID: 31144367. 10: Broere DLJ, Mercado BQ, Lukens JT, Vilbert AC, Banerjee G, Lant HMC, Lee SH, Bill E, Sproules S, Lancaster KM, Holland PL. Reversible Ligand-Centered Reduction in Low-Coordinate Iron Formazanate Complexes. Chemistry. 2018 Jul 2;24(37):9417-9425. doi: 10.1002/chem.201801298. Epub 2018 Jun 7. PMID: 29663542; PMCID: PMC6115202. 11: Mondol R, Otten E. Structure and bonding in reduced boron and aluminium complexes with formazanate ligands. Dalton Trans. 2019 Oct 7;48(37):13981-13988. doi: 10.1039/c9dt02831e. Epub 2019 Aug 16. PMID: 31418002. 12: Travieso-Puente R, Broekman JO, Chang MC, Demeshko S, Meyer F, Otten E. Spin-Crossover in a Pseudo-tetrahedral Bis(formazanate) Iron Complex. J Am Chem Soc. 2016 May 4;138(17):5503-6. doi: 10.1021/jacs.6b01552. Epub 2016 Apr 21. PMID: 27074728. 13: Melenbacher A, Dhindsa JS, Gilroy JB, Stillman MJ. Unveiling the Hidden, Dark, and Short Life of a Vibronic State in a Boron Difluoride Formazanate Dye. Angew Chem Int Ed Engl. 2019 Oct 21;58(43):15339-15343. doi: 10.1002/anie.201908999. Epub 2019 Sep 12. PMID: 31419366. 14: Maar RR, Zhang R, Stephens DG, Ding Z, Gilroy JB. Near-Infrared Photoluminescence and Electrochemiluminescence from a Remarkably Simple Boron Difluoride Formazanate Dye. Angew Chem Int Ed Engl. 2019 Jan 21;58(4):1052-1056. doi: 10.1002/anie.201811144. Epub 2018 Dec 20. PMID: 30485614. 15: Broere DLJ, Mercado BQ, Bill E, Lancaster KM, Sproules S, Holland PL. Alkali Cation Effects on Redox-Active Formazanate Ligands in Iron Chemistry. Inorg Chem. 2018 Aug 20;57(16):9580-9591. doi: 10.1021/acs.inorgchem.8b00226. Epub 2018 Apr 9. PMID: 29629752; PMCID: PMC6116910. 16: Mondol R, Snoeken DA, Chang MC, Otten E. Stable, crystalline boron complexes with mono-, di- and trianionic formazanate ligands. Chem Commun (Camb). 2017 Jan 3;53(3):513-516. doi: 10.1039/c6cc08166e. PMID: 27858024. 17: Maar RR, Barbon SM, Sharma N, Groom H, Luyt LG, Gilroy JB. Evaluation of Anisole-Substituted Boron Difluoride Formazanate Complexes for Fluorescence Cell Imaging. Chemistry. 2015 Oct 26;21(44):15589-99. doi: 10.1002/chem.201502821. Epub 2015 Sep 23. PMID: 26397738. 18: Chang MC, Chantzis A, Jacquemin D, Otten E. Boron difluorides with formazanate ligands: redox-switchable fluorescent dyes with large stokes shifts. Dalton Trans. 2016 Jun 21;45(23):9477-84. doi: 10.1039/c6dt01226d. Epub 2016 May 18. PMID: 27188989. 19: Maar RR, Rabiee Kenaree A, Zhang R, Tao Y, Katzman BD, Staroverov VN, Ding Z, Gilroy JB. Aluminum Complexes of N2O23- Formazanate Ligands Supported by Phosphine Oxide Donors. Inorg Chem. 2017 Oct 16;56(20):12436-12447. doi: 10.1021/acs.inorgchem.7b01907. Epub 2017 Sep 29. PMID: 28960966. 20: Barbon SM, Buddingh JV, Maar RR, Gilroy JB. Boron Difluoride Adducts of a Flexidentate Pyridine-Substituted Formazanate Ligand: Property Modulation via Protonation and Coordination Chemistry. Inorg Chem. 2017 Oct 2;56(19):12003-12011. doi: 10.1021/acs.inorgchem.7b01984. Epub 2017 Sep 18. PMID: 28921960.

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