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1370590-22-9

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

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  • 1370590-22-9 Structure

  • Basic information

    1. Product Name: 2-allylphenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside
    2. Synonyms: 2-allylphenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside
    3. CAS NO:1370590-22-9
    4. Molecular Formula:
    5. Molecular Weight: 464.469
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1370590-22-9.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: 2-allylphenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-allylphenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside(1370590-22-9)
    11. EPA Substance Registry System: 2-allylphenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside(1370590-22-9)

  • 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: 1370590-22-9(Hazardous Substances Data)

1370590-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1370590-22-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,0,5,9 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1370590-22:
(9*1)+(8*3)+(7*7)+(6*0)+(5*5)+(4*9)+(3*0)+(2*2)+(1*2)=149
149 % 10 = 9
So 1370590-22-9 is a valid CAS Registry Number.

1370590-22-9Relevant articles and documents

2-Allylphenyl glycosides as glycosyl donors for sugar coupling

Luo, Shun-Yuan,Tripathi, Ashish,Zulueta, Medel Manuel L.,Hung, Shang-Cheng

experimental part, p. 197 - 201 (2012/06/30)

Glycosylations employing 2-allylphenyl glycoside, a new type of stable glycosyl donor, were optimized and explored with a variety of acceptors promoted by ICl/AgOTf. The utility of the protocol was further demonstrated with an efficient synthesis of the disaccharide fragment of bleomycins.

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