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S-phenyl 2,3-di-O-allyl-4,6-O-benzylidene-1-thia-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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  • 407616-82-4 Structure
  • Basic information

    1. Product Name: S-phenyl 2,3-di-O-allyl-4,6-O-benzylidene-1-thia-α-D-mannopyranoside
    2. Synonyms: S-phenyl 2,3-di-O-allyl-4,6-O-benzylidene-1-thia-α-D-mannopyranoside
    3. CAS NO:407616-82-4
    4. Molecular Formula:
    5. Molecular Weight: 440.56
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 407616-82-4.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: S-phenyl 2,3-di-O-allyl-4,6-O-benzylidene-1-thia-α-D-mannopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: S-phenyl 2,3-di-O-allyl-4,6-O-benzylidene-1-thia-α-D-mannopyranoside(407616-82-4)
    11. EPA Substance Registry System: S-phenyl 2,3-di-O-allyl-4,6-O-benzylidene-1-thia-α-D-mannopyranoside(407616-82-4)
  • 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: 407616-82-4(Hazardous Substances Data)

407616-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 407616-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,7,6,1 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 407616-82:
(8*4)+(7*0)+(6*7)+(5*6)+(4*1)+(3*6)+(2*8)+(1*2)=144
144 % 10 = 4
So 407616-82-4 is a valid CAS Registry Number.

407616-82-4Relevant articles and documents

Synthesis of the mannosyl erythritol lipid MEL A; confirmation of the configuration of the meso-erythritol moiety

Crich, David,De La Mora, Marco A,Cruz, Raymundo

, p. 35 - 44 (2002)

The total synthesis of the two possible diastereomers of mannosylerythritol lipid A, a novel biosurfactant from Candida antartica T-34 with promising anti-proliferative properties in several cell lines, is described. By comparison with an authentic sample

Method of forming glycosidic bonds from thioglycosides using an N,N-dialkylsulfinamide

-

Page 13-14, (2010/02/05)

A method of forming a glycosidic bond utilizing an activated thioglycoside is disclosed. The thioglycoside is activated by an N,N-dialkylsulfinamide and trifluoromethanesulfonic anhydride. The method allows the facile synthesis of disaccharides, oligosacc

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