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89782-10-5

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89782-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89782-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,8 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89782-10:
(7*8)+(6*9)+(5*7)+(4*8)+(3*2)+(2*1)+(1*0)=185
185 % 10 = 5
So 89782-10-5 is a valid CAS Registry Number.

89782-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dihydro-3-(1-imidazolyl)-8-carboxynaphthalene

1.2 Other means of identification

Product number -
Other names 6-Imidazol-1-yl-7,8-dihydro-naphthalene-1-carboxylic acid

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:89782-10-5 SDS

89782-10-5Upstream product

89782-10-5Relevant articles and documents

N-Imidazolyl derivatives of the naphthalene and chroman rings as thromboxane A2 synthase inhibitors

Cozzi, P,Branzoli, U,Carganico, G,Ferti, C,Pillan, A,et al.

, p. 423 - 433 (2007/10/02)

A series of N-imidazol-1-yl derivatives of 1,2-dihydronaphthalene, 1,2,3,4-tetrahydronaphthalene, 2H-1-benzopyran and some related compounds were synthesized and tested as inhibitors of thromboxane A2 synthase in ex vivo experiments with orally treated rats.Some compounds showed good activity which was confirmed in experiments in vitro in rabbit whole blood.Some structural requirements for significant TxA2 synthase inhibitory activity are discussed.The selected 5,6-dihydro-7-(1H-imidazol-1-yl)-2-naphthalene-carboxylic acid (compound 7) was conformationally analysed using the Sybyl molecular model system in comparison with dazoxiben.Compound 7 was further pharmacologically investigated and on the basis of its interesting activities in vitro, ex vivo and in vivo and its low toxicity was selected for clinical investigation.

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