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111570-49-1

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

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  • 111570-49-1 Structure

  • Basic information

    1. Product Name: benzyl 2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside
    2. Synonyms: benzyl 2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside
    3. CAS NO:111570-49-1
    4. Molecular Formula:
    5. Molecular Weight: 660.807
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 111570-49-1.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: benzyl 2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl 2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside(111570-49-1)
    11. EPA Substance Registry System: benzyl 2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside(111570-49-1)

  • 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: 111570-49-1(Hazardous Substances Data)

111570-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111570-49-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,5,7 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 111570-49:
(8*1)+(7*1)+(6*1)+(5*5)+(4*7)+(3*0)+(2*4)+(1*9)=91
91 % 10 = 1
So 111570-49-1 is a valid CAS Registry Number.

111570-49-1Relevant articles and documents

Chemoenzymatic synthesis of ADP-d-glycero-β-d-manno-heptose and study of the substrate specificity of HldE

Li, Tiehai,Wen, Liuqing,Williams, Adriel,Wu, Baolin,Li, Lei,Qu, Jingyao,Meisner, Jeffrey,Xiao, Zhongying,Fang, Junqiang,Wang, Peng George

, p. 1139 - 1147 (2014/02/14)

An efficient one-pot three enzymes strategy for chemoenzymatic synthesis of ADP-d-glycero-β-d-manno-heptose (ADP-d, d-heptose) was reported using chemically synthesized d, d-heptose-7-phosphate and the ADP-d, d-heptose biosynthetic enzymes HldE and GmhB M

Novel synthesis of disaccharides containing the 2-amino-2-deoxy-β-D- glucopyranosyl unit and L-Glycero-D-Manno- and 7-deoxy-L-Glycero-D-Galacto- heptopyranoses

Martin, Patrick,Lequart, Vincent,Cecchelli, Romeo,Boullanger, Paul,Lafont, Dominique,Banoub, Joseph

, p. 696 - 697 (2007/10/03)

Stereocontrolled syntheses of immunologically relevant heptopyranose disaccharides were achieved in excellent yields by the trimethylsilyl triflate promoted glycosylation of the donor 1,3,4,6-tetra-O-acetyl-2-N-allyloxycarbonyl- 2-amino-2-deoxy-β-D-glucop

THE SYNTHESIS OF THE HEPTOSE REGION OF THE GRAM-NEGATIVE BACTERIAL CORE OLIGOSACCHARIDES

Dziewiszek, Krzysztof,Banaszek, Anna,Zamojski, Aleksander

, p. 1569 - 1572 (2007/10/02)

Disaccharides linked α(1-3) and α(1-7) and a trisaccharide linked α(1-7) and α(1-3) have been synthesized from suitably blocked L-glycero-D-mannoheptose derivatives using the trichloroacetimidate approach.

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