MedKoo Cat#: 592117 | Name: Benzalphthalide
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Description:

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

Benzalphthalide has Anti-HIV activity.

Chemical Structure

Benzalphthalide
Benzalphthalide
CAS#575-61-1

Theoretical Analysis

MedKoo Cat#: 592117

Name: Benzalphthalide

CAS#: 575-61-1

Chemical Formula: C15H10O2

Exact Mass: 222.0681

Molecular Weight: 222.24

Elemental Analysis: C, 81.07; H, 4.54; O, 14.40

Price and Availability

Size Price Availability Quantity
5g USD 250.00 2 Weeks
25g USD 550.00 2 Weeks
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Related CAS #
No Data
Synonym
Benzalphthalide; NSC 2824; NSC-2824; NSC2824
IUPAC/Chemical Name
1(3H)-Isobenzofuranone, 3-(phenylmethylene)- (9CI)
InChi Key
YRTPZXMEBGTPLM-UVTDQMKNSA-N
InChi Code
InChI=1S/C15H10O2/c16-15-13-9-5-4-8-12(13)14(17-15)10-11-6-2-1-3-7-11/h1-10H/b14-10-
SMILES Code
O=C1O/C(C2=C1C=CC=C2)=C\C3=CC=CC=C3
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
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 222.24 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: Bedoya LM, del Olmo E, Sancho R, Barboza B, Beltrán M, García-Cadenas AE, Sánchez-Palomino S, López-Pérez JL, Muñoz E, San Feliciano A, Alcamí J. Anti-HIV activity of stilbene-related heterocyclic compounds. Bioorg Med Chem Lett. 2006 Aug 1;16(15):4075-9. Epub 2006 May 18. PubMed PMID: 16713260. 2: Ganji SH, Karigar CS, Pujar BG. Metabolism of benzalphthalide by Pseudomonas sp. World J Microbiol Biotechnol. 1993 Sep;9(5):597-8. doi: 10.1007/BF00386303. PubMed PMID: 24420209. 3: Ganji SH, Pujar BG. Bacterial degradation of benzalphthalide. World J Microbiol Biotechnol. 1992 May;8(3):324-5. doi: 10.1007/BF01201890. PubMed PMID: 24425489.