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ILE-GLY-GLY is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68293-03-8

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68293-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68293-03-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,9 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68293-03:
(7*6)+(6*8)+(5*2)+(4*9)+(3*3)+(2*0)+(1*3)=148
148 % 10 = 8
So 68293-03-8 is a valid CAS Registry Number.

68293-03-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[2-[[(2S,3S)-2-amino-3-methylpentanoyl]amino]acetyl]amino]acetic acid

1.2 Other means of identification

Product number -
Other names Glycine,L-isoleucylglycyl

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:68293-03-8 SDS

68293-03-8Upstream product

68293-03-8Downstream Products

68293-03-8Relevant academic research and scientific papers

Improved solid-phase peptide synthesis method utilizing alpha-azide-protected amino acids.

Lundquist 4th.,Pelletier

, p. 781 - 783 (2001)

[structure: see text]. Pure alpha-azido acids were prepared using an efficient diazo transfer method followed by buffered workup. These building blocks were used to prepare small peptides on Wang resin by two approaches. Peptides prone to diketopiperazine formation were prepared in good yields by coupling acids to resin bound iminophosphoranes during Fmoc-Wang synthesis. The iminophosphoranes can also be hydrolyzed under neutral conditions to provide unprotected amines ready for further coupling.

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