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methyl 4-amino-1H-indazole-1-carboxylate hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

890839-24-4

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890839-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 890839-24-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,0,8,3 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 890839-24:
(8*8)+(7*9)+(6*0)+(5*8)+(4*3)+(3*9)+(2*2)+(1*4)=214
214 % 10 = 4
So 890839-24-4 is a valid CAS Registry Number.

890839-24-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Indazole-1-carboxylic acid, 4-amino-, methyl ester, hydrochloride (1:1)

1.2 Other means of identification

Product number -
Other names 4-Aminoindazole-1-carboxylic acid methyl ester 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:890839-24-4 SDS

890839-24-4Downstream Products

890839-24-4Relevant academic research and scientific papers

Development of a large scale asymmetric synthesis of vanilloid receptor (TRPV1) antagonist ABT-102

Lukin, Kirill,Hsu, Margaret C.,Chambournier, Gilles,Kotecki, Brian,Venkatramani,Leanna

, p. 578 - 584 (2007)

A highly efficient asymmetric synthesis of TRPV1 antagonist ABT-102 was developed and successfully demonstrated on a multi-kilogram scale. This process incorporates a new asymmetric synthesis of (R)-tert-butylaminoindan, which is based on a chiral auxiliary induced diastereoselective reduction of its iminoindan precursor.

Antagonists of the Vanilloid Receptor Subtype 1 (VR1) and Uses Thereof

-

Page/Page column 12, (2008/06/13)

The present invention is directed to compounds of formula (I) wherein variables X1, X2, Y, R1a, R1b, R2a, R2b, A1, A2, A3, and A4 are as defined

Chromanylurea compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor and uses thereof

-

Page/Page column 18, (2008/06/13)

Compounds that are antagonists of the VR1 receptor, having formula (I) [image] or a pharmaceutically acceptable salt, prodrug, or salt of a prodrug thereof, wherein A1, A2, A3, A4, R7, R8, R9, X, Y, Z, L, n, and m, are as defined herein, and are useful in disorders prevented or ameliorated by inhibiting the VR1 receptor.

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