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(3S,4R)-4-Amino-2,2-difluoro-3-hydroxy-5-phenyl-pentanoic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 764628-83-3 Structure
  • Basic information

    1. Product Name: (3S,4R)-4-Amino-2,2-difluoro-3-hydroxy-5-phenyl-pentanoic acid ethyl ester
    2. Synonyms:
    3. CAS NO:764628-83-3
    4. Molecular Formula:
    5. Molecular Weight: 273.28
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 764628-83-3.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: (3S,4R)-4-Amino-2,2-difluoro-3-hydroxy-5-phenyl-pentanoic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3S,4R)-4-Amino-2,2-difluoro-3-hydroxy-5-phenyl-pentanoic acid ethyl ester(764628-83-3)
    11. EPA Substance Registry System: (3S,4R)-4-Amino-2,2-difluoro-3-hydroxy-5-phenyl-pentanoic acid ethyl ester(764628-83-3)
  • 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: 764628-83-3(Hazardous Substances Data)

764628-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 764628-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,4,6,2 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 764628-83:
(8*7)+(7*6)+(6*4)+(5*6)+(4*2)+(3*8)+(2*8)+(1*3)=203
203 % 10 = 3
So 764628-83-3 is a valid CAS Registry Number.

764628-83-3Upstream product

764628-83-3Relevant articles and documents

Peptidyl human heart chymase inhibitors. 1. Synthesis and inhibitory activity of difluoromethylene ketone derivatives bearing P' binding subsites

Eda, Masahiro,Ashimori, Atsuyuki,Akahoshi, Fumihiko,Yoshimura, Takuya,Inoue, Yoshihisa,Fukaya, Chikara,Nakajima, Masahide,Fukuyama, Hajime,Imada, Teruaki,Nakamura, Norifumi

, p. 913 - 918 (1998)

Peptidyl difluoromethylene ketone derivatives were designed to take advantage of probable additional interactions with the S' subsite of human heart chymase. They showed potent inhibitory activities against human heart chymase and were more efficient than bovine chymotrypsin.

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