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1-[(2,2,2-TRICHLOROETHOXY)CARBONYL]-PYRROLIDINE-2-CARBOXYLIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

347386-09-8

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347386-09-8 Usage

Type of Compound

Synthetic chemical compound

Application

Used as an antimicrobial agent in personal care products such as soaps and lotions

Function

Inhibits the growth of bacteria on the skin

Purpose

Effective ingredient in products designed to prevent the spread of germs and infections

Health Concerns

Linked to potential hormonal disruption

Environmental Concerns

Linked to potential antibiotic resistance

Regulatory Status

Use has been restricted in some countries

Ongoing Efforts

Efforts are being made to find safer alternatives for antimicrobial protection in personal care products.

Check Digit Verification of cas no

The CAS Registry Mumber 347386-09-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,7,3,8 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 347386-09:
(8*3)+(7*4)+(6*7)+(5*3)+(4*8)+(3*6)+(2*0)+(1*9)=168
168 % 10 = 8
So 347386-09-8 is a valid CAS Registry Number.

347386-09-8SDS

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 1-(2,2,2-trichloroethoxycarbonyl)pyrrolidine-2-carboxylic acid

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:347386-09-8 SDS

347386-09-8Downstream Products

347386-09-8Relevant academic research and scientific papers

Chemical conversion of cyclic α-amino acids to cyclic α-aminophosphonic acids

Kaname,Mashige,Yoshifuji

, p. 531 - 536 (2001)

The oxidative decarboxylation of cyclic α-amino acids having urethane-type N-protecting groups with lead tetraacetate [Pb(OAc)4] gave 2-hydroxy derivatives, which were transformed into the corresponding α-aminophosphonic acid esters by treatment of trialkyl phosphites in the presence of Lewis acids. Deprotection and ester cleavage of the products in the usual manner afforded cyclic α-aminophosphonic acids. The convenient chemical conversion of five- and six-membered cyclic α-amino acids to the corresponding cyclic α-aminophosphonic acids has been accomplished.

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