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167113-73-7

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167113-73-7 Usage

Uses

2-(Ethoxycarbonyl)cyclopropane-1-carboxylic Acid, is a building block used in various chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 167113-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,1,1 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 167113-73:
(8*1)+(7*6)+(6*7)+(5*1)+(4*1)+(3*3)+(2*7)+(1*3)=127
127 % 10 = 7
So 167113-73-7 is a valid CAS Registry Number.

167113-73-7SDS

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 2-(Ethoxycarbonyl)cyclopropanecarboxylic acid

1.2 Other means of identification

Product number -
Other names (2-(4-(tert-butyldimethylsilyloxy)phenyl)-6-hydroxybenzo[b]thiophen-3-yl)(4-(2-(piperidin-1-yl)ethoxy)phenyl)methanone

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:167113-73-7 SDS

167113-73-7Relevant articles and documents

USE OF T-TYPE CALCIUM CHANNEL BLOCKER FOR TREATING PRURITUS

-

, (2022/02/19)

A medicament for treating or preventing pruritus is provided. For the medicament for treating or preventing pruritus, a compound having a blocking action on Cav3.2T-type calcium channels represented by General Formulas (I) to (VI), a tautomer of the compo

Fibrinogen receptor antagonists

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, (2008/06/13)

Fibrinogen receptor antagonists having the formula STR1 for example STR2

Substituted heterocyclic derivatives useful as platelet aggregation inhibitors

-

, (2008/06/13)

Novel substituted heterocyclic derivatives are provided which inhibit platelet aggregation. This invention also pertains to pharmaceutical compositions and methods of using such derivatives.

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