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4-chlorophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-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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  • 85951-18-4 Structure
  • Basic information

    1. Product Name: 4-chlorophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-mannopyranoside
    2. Synonyms: 4-chlorophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-mannopyranoside
    3. CAS NO:85951-18-4
    4. Molecular Formula:
    5. Molecular Weight: 474.916
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85951-18-4.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: 4-chlorophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-mannopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-chlorophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-mannopyranoside(85951-18-4)
    11. EPA Substance Registry System: 4-chlorophenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-mannopyranoside(85951-18-4)
  • 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: 85951-18-4(Hazardous Substances Data)

85951-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85951-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,5 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85951-18:
(7*8)+(6*5)+(5*9)+(4*5)+(3*1)+(2*1)+(1*8)=164
164 % 10 = 4
So 85951-18-4 is a valid CAS Registry Number.

85951-18-4Downstream Products

85951-18-4Relevant articles and documents

InBr 3 -Catalyzed Synthesis of Aryl 1,2- trans -Thio(seleno)glycosides

Ma, Teng,Li, Changwei,Liang, Haijing,Wang, Zhaoyan,Yu, Lan,Xue, Weihua

, p. 2311 - 2314 (2017)

InBr 3 is demonstrated to be an efficient catalyst for reactions of fully acetated aldoses with aryl mercaptans or selenophenol at room temperature, rapidly furnishing the corresponding thioglycosides or selenoglycosides with exclusively 1,2- t

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