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Glycine, N-2-pyrimidinyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79858-46-1

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79858-46-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79858-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,5 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79858-46:
(7*7)+(6*9)+(5*8)+(4*5)+(3*8)+(2*4)+(1*6)=201
201 % 10 = 1
So 79858-46-1 is a valid CAS Registry Number.

79858-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(pyrimidin-2-ylamino)acetic acid

1.2 Other means of identification

Product number -
Other names Glycine,N-2-pyrimidinyl

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:79858-46-1 SDS

79858-46-1Downstream Products

79858-46-1Relevant academic research and scientific papers

Solid-phase synthesis of methyl N-(pyrimidin-2-yl)glycinate

Ermolat'ev, Denis S.,Babaev, Eugene V.

, p. 467 - 471 (2003)

A versatile method for the preparation of N-heteroaryl substituted aminoacid derivatives is suggested. The method avoids facile diketopiperazine formation.

Basic techniques of working on a solid phase: From ABC of the peptide synthesis to libraries of non-natural amino acids

Babaev,Ermolat'ev

experimental part, p. 2572 - 2589 (2011/04/15)

Libraries of hardly available amino acids bearing a heteroaromatic ring (2-pyrimidyl, substituted 2-pyridyl or 2-thiazolyl) at the amino group were prepared using solid-phase synthesis on various resins. The synthesized compounds are structurally similar to some known antidiabetic drugs. The paper combines features of a review (elementary introduction to the solid-phase synthesis methodology and technique for beginners and selected methods from peptide chemistry) and step-by-step experimental protocols (tested by the authors) useful as a methodic tool. The presented protocols (immobilization and modification of amino acids, placing and removal of common protective groups) require no sophisticated equipment and may be useful as pictorial introductory tasks for students education. Pleiades Publishing, Ltd., 2010.

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