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2-(3-tert-butoxycarbonylaminopropionylamino)-3-(1-trityl-1H-imidazol-4-yl)propionic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

952739-80-9

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952739-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 952739-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,2,7,3 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 952739-80:
(8*9)+(7*5)+(6*2)+(5*7)+(4*3)+(3*9)+(2*8)+(1*0)=209
209 % 10 = 9
So 952739-80-9 is a valid CAS Registry Number.

952739-80-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-tert-butoxycarbonylaminopropionylamino)-3-(1-trityl-1H-imidazol-4-yl)propionic acid methyl ester

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:952739-80-9 SDS

952739-80-9Downstream Products

952739-80-9Relevant academic research and scientific papers

An expedient, scalable synthesis of the natural product L-anserine

Wiles, Charlotte,Watts, Paul

, p. 2608 - 2610 (2008/02/13)

To date, the synthesis of L-anserine has relied on the use of naturally occurring 1-methyl-L-histidine as a precursor, however its high cost prevents its use in the large-scale synthesis of L-anserine. With this in mind, we report herein a concise and efficient synthetic strategy, employing the 160-fold less expensive, L-histidine methyl ester dihydrochloride as a starting material, to afford the title compound in an overall yield of 88%, over four reaction steps. Georg Thieme Verlag Stuttgart.

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