Welcome to LookChem.com Sign In|Join Free

CAS

  • or

213316-32-6

Post Buying Request

213316-32-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • Cyclopropanecarboxylic acid, 1-amino-2-ethenyl-, ethyl ester, (1R,2S)-rel- (9CI)

    Cas No: 213316-32-6

  • No Data

  • No Data

  • No Data

  • BOC Sciences
  • Contact Supplier

213316-32-6 Usage

General Description

Cyclopropanecarboxylic acid, 1-amino-2-ethenyl-, ethyl ester, (1R,2S)-rel- (9CI) is a chemical compound with a molecular formula C7H11NO2. It is a derivative of cyclopropanecarboxylic acid and is classified as an ethyl ester. Cyclopropanecarboxylic acid, 1-amino-2-ethenyl-, ethyl ester, (1R,2S)-rel- (9CI) contains an amino group and an ethenyl group, and its stereochemistry is designated as (1R,2S)-rel-. It is commonly used in chemical synthesis and research as a reagent and intermediate. The properties and uses of this compound in various industries and applications may vary depending on the specific stereochemistry and the reactions in which it is involved.

Check Digit Verification of cas no

The CAS Registry Mumber 213316-32-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,3,1 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 213316-32:
(8*2)+(7*1)+(6*3)+(5*3)+(4*1)+(3*6)+(2*3)+(1*2)=86
86 % 10 = 6
So 213316-32-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO2/c1-3-6-5-8(6,9)7(10)11-4-2/h3,6H,1,4-5,9H2,2H3/t6-,8-/m1/s1

213316-32-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclopropanecarboxylic acid, 1-amino-2-ethenyl-, ethyl ester, (1R,2S)-rel-

1.2 Other means of identification

Product number -
Other names -

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:213316-32-6 SDS

213316-32-6Downstream Products

213316-32-6Relevant articles and documents

CALPAIN MODULATORS AND METHODS OF PRODUCTION AND USE THEREOF

-

, (2017/09/27)

The present technology relates to compounds, kits, compositions, and methods useful for the treatment of fibrotic disease. In some aspects, the present technology provides for treatment of various diseases or disorders associated or mediated, at least in part, by calpains, such as CAPN1, CAPN2, and/or CAPN9. The present technology is generally applicable to compounds which inhibit myofibroblast differentiation.

Macrocyclic compounds for suppressing replication of hepatitis C virus

-

Page/Page column 39; 40, (2016/05/24)

A compound as represented by Formula (I) is provided, wherein groups are defined in the description. The compound is used as HCV protease inhibitor for treating HCV infection.

Dynamic kinetic resolution of dehydrocoronamic acid

Chaplin, David A.,Fox, Martin E.,Kroll, Sebastian H. B.

supporting information, p. 5858 - 5860 (2014/05/20)

Dehydrocoronamic acid can be racemised by dehydration of an N-acyl derivative to an azlactone, which undergoes facile racemisation. For the N-trifluoroacetyl derivative, the racemisation process was combined with an enzymatic resolution, to achieve a dynamic kinetic resolution process by which the racemate can be converted to either enantiomer. This journal is the Partner Organisations 2014.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 213316-32-6