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167904-03-2

2,3,4,6-tetra-O-benzyl-D-galactononitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 167904-03-2 Structure

  • Basic information

    1. Product Name: 2,3,4,6-tetra-O-benzyl-D-galactononitrile
    2. Synonyms: 2,3,4,6-tetra-O-benzyl-D-galactononitrile
    3. CAS NO:167904-03-2
    4. Molecular Formula:
    5. Molecular Weight: 537.656
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 167904-03-2.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: 2,3,4,6-tetra-O-benzyl-D-galactononitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3,4,6-tetra-O-benzyl-D-galactononitrile(167904-03-2)
    11. EPA Substance Registry System: 2,3,4,6-tetra-O-benzyl-D-galactononitrile(167904-03-2)

  • 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: 167904-03-2(Hazardous Substances Data)

167904-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 167904-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,9,0 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 167904-03:
(8*1)+(7*6)+(6*7)+(5*9)+(4*0)+(3*4)+(2*0)+(1*3)=152
152 % 10 = 2
So 167904-03-2 is a valid CAS Registry Number.

167904-03-2Relevant articles and documents

40. Synthesis of galactose- and N-acetylglucosamine-derived tetrazoles and their evaluation as β-glycosidase inhibitors

Heightman,Ermert,Klein,Vasella

, p. 514 - 532 (1995)

The title compounds 6 and 7 have been prepared from the known 2,3-di-O-benzyl-4,6-O-benzylidene-D-galactose (18) and N2-acetyl-tri-O-benzyl-D-glucosamine oxime (29) in eight and six steps, respectively. The azidonitrile leading to the benzylate

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