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L-Valine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-isoleucyl]-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75922-53-1

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75922-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75922-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,2 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75922-53:
(7*7)+(6*5)+(5*9)+(4*2)+(3*2)+(2*5)+(1*3)=151
151 % 10 = 1
So 75922-53-1 is a valid CAS Registry Number.

75922-53-1SDS

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 N-(t-butoxycarbonyl)isoleucylvaline benzyl ester

1.2 Other means of identification

Product number -
Other names (S)-2-((2S,3S)-2-tert-Butoxycarbonylamino-3-methyl-pentanoylamino)-3-methyl-butyric acid benzyl ester

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:75922-53-1 SDS

75922-53-1Relevant academic research and scientific papers

Peptide Synthesis in Aqueous Solution. V. Properties and Reactivities of (p-Hydroxyphenyl)benzylmethylsulfonium Salts for Direct Benzyl Esterification of N-Acylpeptides

Nakata, Takashi,Nakatani, Masaru,Takahashi, Masatoshi,Okai, Jiro,Kawaoka, Yoshiaki,Kouge, Katsushige,Okai, Hideo

, p. 1099 - 1106 (2007/10/03)

Some (p-hydroxyphenyl)benzylmethylsulfonium salts were prepared. These compounds generated a benzyl cation and converted not only N-acylamino acids but also N-acylpeptides into their corresponding benzyl esters without causing the racemization.

MIXED ANHYDRIDES IN PEPTIDE SYNTHESIS. A STUDY URETHANE FORMATION WITH A CONTRIBUTION ON MINIMIZATION OF RACEMIZATION

Chen, Francis M. F.,Lee, Young,Steinauer, Rene,Benoiton, N. Leo

, p. 613 - 618 (2007/10/02)

A study of the factors contributing to urethane formation during the coupling of N-alkoxycarbonylamino acids with an amino acid ester by the mixed carboxylic-carbonic acid anhydride method has been carried out, using nuclear magnetic resonance spectroscop

Studies of Bitter Peptides from Casein Hydrolyzate. I. Synthesis of Bitter Peptide BPIa Corresponding to Arg-Gly-Pro-Pro-Phe-Ile-Val from Casein Hydrolyzate by Alkaline Proteinase of Bacillus subtilis

Fukui, Hiroshi,Kanehisa, Hidenori,Ishibashi, Norio,Miyake, Ichizo,Okai, Hideo

, p. 766 - 769 (2007/10/02)

A bitter heptapeptide BPIa was synthesized and compared with the natural peptide, isolated by Minamiura et al. from casein hydrolyzate, by means of thin layer chromatography, paper electrophoresis, and carboxymethylcellulose column chromatography.All resu

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