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4-benzyl(benzyloxycarbonyl)amino-4,5-dideoxy-2,3-O-(1-methylethylidene)-5-phenylthio-D-xylose diethyl dithioacetal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133760-18-6 Structure
  • Basic information

    1. Product Name: 4-benzyl(benzyloxycarbonyl)amino-4,5-dideoxy-2,3-O-(1-methylethylidene)-5-phenylthio-D-xylose diethyl dithioacetal
    2. Synonyms:
    3. CAS NO:133760-18-6
    4. Molecular Formula:
    5. Molecular Weight: 611.891
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133760-18-6.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: 4-benzyl(benzyloxycarbonyl)amino-4,5-dideoxy-2,3-O-(1-methylethylidene)-5-phenylthio-D-xylose diethyl dithioacetal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-benzyl(benzyloxycarbonyl)amino-4,5-dideoxy-2,3-O-(1-methylethylidene)-5-phenylthio-D-xylose diethyl dithioacetal(133760-18-6)
    11. EPA Substance Registry System: 4-benzyl(benzyloxycarbonyl)amino-4,5-dideoxy-2,3-O-(1-methylethylidene)-5-phenylthio-D-xylose diethyl dithioacetal(133760-18-6)
  • 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: 133760-18-6(Hazardous Substances Data)

133760-18-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133760-18-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,7,6 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 133760-18:
(8*1)+(7*3)+(6*3)+(5*7)+(4*6)+(3*0)+(2*1)+(1*8)=116
116 % 10 = 6
So 133760-18-6 is a valid CAS Registry Number.

133760-18-6Relevant articles and documents

Enantiospecific synthesis of polyoxamic acid from L-arabinose

Dureault,Carreaux,Depezay

, p. 150 - 155 (1991)

An enantiospecific synthesis of polyoxamic acid, 2-amino-2-deoxy-L-xylonic acid, by phenylthiolate opening of a five-carbon chiral hydroxylated aziridine easily derived from L-arabinose, is reported. The formation of the carboxyl group resulted from a Pum

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