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3,7-anhydro-1-deoxy-2-O-p-tolylsulfonyl-D-threo-L-talo-octitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 91738-18-0 Structure
  • Basic information

    1. Product Name: 3,7-anhydro-1-deoxy-2-O-p-tolylsulfonyl-D-threo-L-talo-octitol
    2. Synonyms:
    3. CAS NO:91738-18-0
    4. Molecular Formula:
    5. Molecular Weight: 362.401
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91738-18-0.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: 3,7-anhydro-1-deoxy-2-O-p-tolylsulfonyl-D-threo-L-talo-octitol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,7-anhydro-1-deoxy-2-O-p-tolylsulfonyl-D-threo-L-talo-octitol(91738-18-0)
    11. EPA Substance Registry System: 3,7-anhydro-1-deoxy-2-O-p-tolylsulfonyl-D-threo-L-talo-octitol(91738-18-0)
  • 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: 91738-18-0(Hazardous Substances Data)

91738-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91738-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,3 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91738-18:
(7*9)+(6*1)+(5*7)+(4*3)+(3*8)+(2*1)+(1*8)=150
150 % 10 = 0
So 91738-18-0 is a valid CAS Registry Number.

91738-18-0Relevant articles and documents

Reactions of Enolic Sugar Derivatives, XVI. - Synthesis of a Diastereotopic Proton Probe for α- and β-D-Glucosylases

Brewer, Curtis F.,Hehre, Edward J.,Lehmann, Jochen,Weiser, Wolfgang

, p. 1078 - 1087 (2007/10/02)

For the elucidation of the stereochemistry in glucosylase-catalyzed proton addition reactions (Z)-3,7-anhydro-1,2-dideoxy-D-gluco-oct-2-enitol (1) was synthesized.Starting material for the multistep synthesis is 3,4,5,7-tetra-O-acetyl-2,6-anhydro-1-C-(1,3

DIASTEREOTOPIC SUBSTRATES OF β-D-GALACTOSIDASE FROM Escherichia coli AS PROBES FOR A CATALYTICALLY ACTIVE, PROTONATING GROUP

Fritz, Hans,Lehmann, Jochen,Schlesselmann, Peter

, p. 71 - 92 (2007/10/02)

With 3,4,5,7-tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptonitrile as the starting material, the diastereotopic, enolic sugar derivatives (Z)-3,7-anhydro-2-deoxy-D-galacto-oct -2-enononitrile (2) and (Z)- (5) and (E)-3,7-anhydro-1,2-dideoxy-D-galacto-

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