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(S)-6-benzyl 1-methyl 2-((tert-butoxycarbonyl)amino)-4-oxohexanedioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1379524-31-8 Structure
  • Basic information

    1. Product Name: (S)-6-benzyl 1-methyl 2-((tert-butoxycarbonyl)amino)-4-oxohexanedioate
    2. Synonyms:
    3. CAS NO:1379524-31-8
    4. Molecular Formula:
    5. Molecular Weight: 379.41
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1379524-31-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-6-benzyl 1-methyl 2-((tert-butoxycarbonyl)amino)-4-oxohexanedioate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-6-benzyl 1-methyl 2-((tert-butoxycarbonyl)amino)-4-oxohexanedioate(1379524-31-8)
    11. EPA Substance Registry System: (S)-6-benzyl 1-methyl 2-((tert-butoxycarbonyl)amino)-4-oxohexanedioate(1379524-31-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1379524-31-8(Hazardous Substances Data)

1379524-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1379524-31-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,5,2 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1379524-31:
(9*1)+(8*3)+(7*7)+(6*9)+(5*5)+(4*2)+(3*4)+(2*3)+(1*1)=188
188 % 10 = 8
So 1379524-31-8 is a valid CAS Registry Number.

1379524-31-8Relevant articles and documents

Developing diazirine-based chemical probes to identify histone modification 'readers' and 'erasers'

Yang, Tangpo,Liu, Zheng,Li, Xiang David

, p. 1011 - 1017 (2015)

Post translational modifications (PTMs, e.g., phosphorylation, acetylation and methylation) of histone play important roles in regulating many fundamental cellular processes such as gene transcription, DNA replication and damage repair. While 'writer' and

Enantiopure synthesis of side chain-modified α-amino acids and 5-cis-alkylprolines

Mohite, Amar R.,Bhat, Ramakrishna G.

, p. 5423 - 5428 (2012/08/28)

A short, concise synthesis of enantiopure, side chain-modified α-amino acids such as 4-oxo-l-norvaline, 6-oxo-l-homonorleucine, and 5-cis-alkyl prolines is described. Knoevenagel condensation of l-aminocarboxylate-derived β-ketoesters with aldehydes followed by reductive decarboxylation results in unnatural α-amino acids in good yield. A fluorescent amino acid is synthesized using a similar protocol. These studies show that aminocarboxylate-derived β-ketoesters are very useful intermediates and the method employed is both general and practical for the preparation of γ(δ)-oxo α-amino acids and alkylprolines.

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