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CAS

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910642-66-9

(S)-[3-Chloro-2-oxo-1-(phenylmethyl)propyl]-carbamic acid,1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 910642-66-9 Structure

  • Basic information

    1. Product Name: (S)-[3-Chloro-2-oxo-1-(phenylmethyl)propyl]-carbamic acid,1,1-dimethylethyl ester
    2. Synonyms: (S)-[3-Chloro-2-oxo-1-(phenylmethyl)propyl]-carbamic acid,1,1-dimethylethyl ester
    3. CAS NO:910642-66-9
    4. Molecular Formula:
    5. Molecular Weight: 297.782
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 910642-66-9.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)-[3-Chloro-2-oxo-1-(phenylmethyl)propyl]-carbamic acid,1,1-dimethylethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-[3-Chloro-2-oxo-1-(phenylmethyl)propyl]-carbamic acid,1,1-dimethylethyl ester(910642-66-9)
    11. EPA Substance Registry System: (S)-[3-Chloro-2-oxo-1-(phenylmethyl)propyl]-carbamic acid,1,1-dimethylethyl ester(910642-66-9)

  • 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: 910642-66-9(Hazardous Substances Data)

910642-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 910642-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,6,4 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 910642-66:
(8*9)+(7*1)+(6*0)+(5*6)+(4*4)+(3*2)+(2*6)+(1*6)=149
149 % 10 = 9
So 910642-66-9 is a valid CAS Registry Number.

910642-66-9Relevant articles and documents

Processes for producing α-halo ketones, α-halohydrins and epoxides

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, (2008/06/13)

Processes for efficiently producing α-halo ketones, α-halohydrins and epoxides on an industrial scale. The prosesses include one for producing an α-halo ketone of general formula (3) by decarboxylating a product of reaction between a carboxilic acid derivative of general formula (1) and a metal enolate prepared from an α-haloacetic acid of general formula (2) or an acceptable salt thereof, one for producing an by reducing the α-halo ketone (3), and one for producing an epoxide (13) by treating the α-halohydrin (11) with a base to effect ring closure. The above prosesses are particularly suitable for producing optically active α-halo ketones, α-halohydrins and epoxides from the corresponding α-amino acid derivatives. STR1

Ureido amino and imino acids, compositions and methods for use

-

, (2008/06/13)

Compounds of the formula STR1 wherein X is various amino or imino acids and esters are disclosed. These compounds are useful due to their angiotensin converting enzyme inhibition activity and depending upon the definition of X may also be useful as analge

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