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Cyclobutanecarboxylic acid, 2-amino-3-hydroxy-, (1S,2S,3R)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

349102-18-7

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349102-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 349102-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,9,1,0 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 349102-18:
(8*3)+(7*4)+(6*9)+(5*1)+(4*0)+(3*2)+(2*1)+(1*8)=127
127 % 10 = 7
So 349102-18-7 is a valid CAS Registry Number.

349102-18-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2S,3R)-2-amino-3-hydroxycyclobutane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names Cyclobutanecarboxylic acid,2-amino-3-hydroxy-,(1S,2S,3R)-(9CI)

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:349102-18-7 SDS

349102-18-7Upstream product

349102-18-7Downstream Products

349102-18-7Relevant academic research and scientific papers

Stereocontrolled preparation of diversely trifunctionalized cyclobutanes

Aitken, David J.,Boddaert, Thomas,Chang, Zong,Guillot, Régis

, (2019)

The expedient and stereoselective syntheses of small libraries of trifunctionalized cyclobutane scaffolds bearing an acid, an amine, and a third functional group are described. Starting from a single precursor, the readily available protected derivative of all-cis-2-amino-3-hydroxycyclobutane-1-carboxylic acid, cis-trans stereoisomers are obtained following an SN2-type reaction, while all-trans stereoisomers are obtained using the same strategy preceded by a C1 epimerization reaction.

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