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110683-23-3

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110683-23-3 Usage

General Description

8-Amino-4-oxo-2-tetrazol-5-yl-4H-1-benzopyran is a chemical compound with the molecular formula C10H8N6O2. It is a derivative of benzopyran, containing an amino group and a tetrazolyl group. 8-Amino-4-oxo-2-tetrazol-5-yl-4H-1-benzopyran has potential pharmacological properties, and research has shown that it may have anticancer, anti-inflammatory, and antimicrobial activities. It is also being studied for its potential use in treating neurodegenerative diseases and as a component in drug development. 8-Amino-4-oxo-2-tetrazol-5-yl-4H-1-benzopyran has the potential to be a valuable compound in medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 110683-23-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,6,8 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 110683-23:
(8*1)+(7*1)+(6*0)+(5*6)+(4*8)+(3*3)+(2*2)+(1*3)=93
93 % 10 = 3
So 110683-23-3 is a valid CAS Registry Number.

110683-23-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-amino-2-(2H-tetrazol-5-yl)chromen-4-one,hydrochloride

1.2 Other means of identification

Product number -
Other names 8-amino-4-oxo-tetrazol-5-yl-4H-1-benzopyran hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:110683-23-3 SDS

110683-23-3Downstream Products

110683-23-3Relevant articles and documents

New potent antagonists of leukotrienes C4 and D4. 1. Synthesis and structure-activity relationships

Nakai,Konno,Kosuge,Sakuyama,Toda,Arai,Obata,Katsube,Miyamoto,Okegawa,Kawasaki

, p. 84 - 91 (2007/10/02)

(p-Amylcinnamoyl)anthranilic acid (3a) had moderate antagonist activities against LTD4-induced smooth muscle contraction on guinea pig ileum and LTC4-induced bronchoconstriction in anesthetized guinea pigs. Modifications were made in the hydrophobic part (cinnamoyl moiety) and the hydrophilic part (anthranilate moiety) of 3a. A series of 8-(benzoylamino)-2-tetrazol-5-yl-1,4-benzodioxans and 8-(benzoylamino)-2-tetrazol-5-yl-4-oxo-4H-1-benzopyrans were revealed to be potent antagonists of leukotrienes C4 and D4. Among both series, ONO-RS-347 (18k) and ONO-RS411 (19h) were the most potent and orally active antagonists, respectively. Structure-activity relationships are discussed.

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