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150969-30-5

2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl trichloroacetimidate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 150969-30-5 Structure

  • Basic information

    1. Product Name: 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl trichloroacetimidate
    2. Synonyms: 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl trichloroacetimidate
    3. CAS NO:150969-30-5
    4. Molecular Formula:
    5. Molecular Weight: 592.903
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 150969-30-5.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-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl trichloroacetimidate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl trichloroacetimidate(150969-30-5)
    11. EPA Substance Registry System: 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl trichloroacetimidate(150969-30-5)

  • 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: 150969-30-5(Hazardous Substances Data)

150969-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150969-30-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,9,6 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 150969-30:
(8*1)+(7*5)+(6*0)+(5*9)+(4*6)+(3*9)+(2*3)+(1*0)=145
145 % 10 = 5
So 150969-30-5 is a valid CAS Registry Number.

150969-30-5Relevant articles and documents

Synthesis of α-galactosyl ceramide, a potent immunostimulatory agent

Plettenburg, Oliver,Bodmer-Narkevitch, Vera,Wong, Chi-Huey

, p. 4559 - 4564 (2007/10/03)

α-Galactosyl ceramide has been identified to be a potent stimulatory agent for a novel immunological process, mediated by CD1 molecules. This paper describes a short and efficient synthesis of α-galactosyl ceramide. Starting from commercially available 2-deoxy galactose, a suitable sphingosine derivative was obtained in nine steps and 36% overall yield, which was subsequently glycosylated to give the target molecule. This flexible route will provide various glycolipids for further exploration of this interesting biological process.

Synthesis of structural elements of the capsular polysaccharide of Streptococcus pneumoniae type 8

Koeman,Kamerling,Vliegenthart

, p. 5291 - 5304 (2007/10/02)

The synthesis is reported of propyl 4-O-α-D-galactopyranosyl-β-D-glucopyranosiduronic acid (25), 4-O-[4-O-(β-D-glucopyranosyluronic acid)-β-D-glucopyranosyl]-D-glucopyranose (34) and 4-O-(4-O-β-D-glucopyranosyl-α-D-glucopyranosyl)-D-galactopyranose (38),

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