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ethyl N-benzyloxycarbonyl-L-2-amino-5-hexenoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 241161-72-8 Structure
  • Basic information

    1. Product Name: ethyl N-benzyloxycarbonyl-L-2-amino-5-hexenoate
    2. Synonyms:
    3. CAS NO:241161-72-8
    4. Molecular Formula:
    5. Molecular Weight: 291.347
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 241161-72-8.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: ethyl N-benzyloxycarbonyl-L-2-amino-5-hexenoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl N-benzyloxycarbonyl-L-2-amino-5-hexenoate(241161-72-8)
    11. EPA Substance Registry System: ethyl N-benzyloxycarbonyl-L-2-amino-5-hexenoate(241161-72-8)
  • 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: 241161-72-8(Hazardous Substances Data)

241161-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 241161-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,1,1,6 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 241161-72:
(8*2)+(7*4)+(6*1)+(5*1)+(4*6)+(3*1)+(2*7)+(1*2)=98
98 % 10 = 8
So 241161-72-8 is a valid CAS Registry Number.

241161-72-8Relevant articles and documents

A simple modular synthesis of pyridinoline a collagen cross-link of biochemical interest

Allevi, Pietro,Anastasia, Mario

, p. 2005 - 2012 (2003)

A simple convergent synthesis of the collagen cross-link pyridinoline starting from glycine is reported.

A Strategy Towards the Stereoselective Synthesis of 5-Hydroxylysine

Loehr, Birgit,Orlich, Simone,Kunz, Horst

, p. 1139 - 1141 (2007/10/03)

A stereoselective synthesis of 5-hydroxylysine is described in which the α-stereogenic centre is generated by a Schoellkopf amino acid synthesis, and the ethanolamine structure is obtained via Sharpless aminohydroxylation from an olefin moiety. The reactions and their selectivities are studied.

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