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1379780-08-1

Ac-Trp(Boc)-Met-Asp(t-Bu)-Phe-NH2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1379780-08-1 Structure

  • Basic information

    1. Product Name: Ac-Trp(Boc)-Met-Asp(t-Bu)-Phe-NH2
    2. Synonyms: Ac-Trp(Boc)-Met-Asp(t-Bu)-Phe-NH2
    3. CAS NO:1379780-08-1
    4. Molecular Formula:
    5. Molecular Weight: 794.97
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1379780-08-1.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: Ac-Trp(Boc)-Met-Asp(t-Bu)-Phe-NH2(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ac-Trp(Boc)-Met-Asp(t-Bu)-Phe-NH2(1379780-08-1)
    11. EPA Substance Registry System: Ac-Trp(Boc)-Met-Asp(t-Bu)-Phe-NH2(1379780-08-1)

  • 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: 1379780-08-1(Hazardous Substances Data)

1379780-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1379780-08-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,7,8 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1379780-08:
(9*1)+(8*3)+(7*7)+(6*9)+(5*7)+(4*8)+(3*0)+(2*0)+(1*8)=211
211 % 10 = 1
So 1379780-08-1 is a valid CAS Registry Number.

1379780-08-1Upstream product

1379780-08-1Downstream Products

1379780-08-1Relevant articles and documents

Enzymatic C-terminal amidation of amino acids and peptides

Nuijens, Timo,Piva, Elena,Kruijtzer, John A.W.,Rijkers, Dirk T.S.,Liskamp, Rob M.J.,Quaedflieg, Peter J.L.M.

, p. 3777 - 3779 (2012)

Herein, we describe two versatile and high yielding enzymatic approaches for the conversion of semi-protected amino acid and peptidyl C-terminal α-carboxylic acids into their corresponding amides. In the first approach, the lipase Candida antarctica lipase-B (Cal-B), and in the second approach, the protease Subtilisin A, are used, respectively. We found that by using the ammonium salt of the α-carboxylic acid instead of separate ammonia sources, the enzymatic amidation reactions proceeded much faster without side reactions and gave near to quantitative yields of products.

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