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CAS

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122689-83-2

(3R,5R)-3-Benzyloxycarbonylmethyl-2-oxo-5-phenyl-morpholine-4-carboxylic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 122689-83-2 Structure

  • Basic information

    1. Product Name: (3R,5R)-3-Benzyloxycarbonylmethyl-2-oxo-5-phenyl-morpholine-4-carboxylic acid tert-butyl ester
    2. Synonyms:
    3. CAS NO:122689-83-2
    4. Molecular Formula:
    5. Molecular Weight: 425.481
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122689-83-2.mol
    9. Article Data: 1

  • 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: (3R,5R)-3-Benzyloxycarbonylmethyl-2-oxo-5-phenyl-morpholine-4-carboxylic acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R,5R)-3-Benzyloxycarbonylmethyl-2-oxo-5-phenyl-morpholine-4-carboxylic acid tert-butyl ester(122689-83-2)
    11. EPA Substance Registry System: (3R,5R)-3-Benzyloxycarbonylmethyl-2-oxo-5-phenyl-morpholine-4-carboxylic acid tert-butyl ester(122689-83-2)

  • 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: 122689-83-2(Hazardous Substances Data)

122689-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122689-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,6,8 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 122689-83:
(8*1)+(7*2)+(6*2)+(5*6)+(4*8)+(3*9)+(2*8)+(1*3)=142
142 % 10 = 2
So 122689-83-2 is a valid CAS Registry Number.

122689-83-2Downstream Products

122689-83-2Relevant articles and documents

STEREOSELECTIVE ALKYLATION OF CHIRAL GLYCINE ENOLATE SYNTHONS. THE ENANTIOSELECTIVE SYNTHESIS O α-AMINO ACID DERIVATES

Dellaria, Joseph F.,Santarsiero, Bernard D.

, p. 6079 - 6082 (2007/10/02)

The highly stereoselective alkylation (percentde=99.6 to 97.6) o a new chiral glycine enolate synthon derived from D-2-phenylglycinol is described.Deprotection of the alkylation adducts in a one-pot, three-step procedure provides the ethyl ester hydrochloride salts of the corresponding α-amino acids with no attending racemization.

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