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C-(2,3,4,6-TETRA-O-ACETYL-1-BROMO-1-DEOXY-BETA-D-GALACTOPYRANOSYL)FORMAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • C-(2,3,4,6-TETRA-O-ACETYL-1-BROMO-1-DEOXY-BETA-D-GALACTOPYRANOSYL)FORMAMIDE

    Cas No: 159895-07-5

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  • C-(2,3,4,6-TETRA-O-ACETYL-1-BROMO-1-DEOXY-BETA-D-GALACTOPYRANOSYL)FORMAMIDE

    Cas No: 159895-07-5

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  • 159895-07-5 Structure
  • Basic information

    1. Product Name: C-(2,3,4,6-TETRA-O-ACETYL-1-BROMO-1-DEOXY-BETA-D-GALACTOPYRANOSYL)FORMAMIDE
    2. Synonyms: C-(2,3,4,6-TETRA-O-ACETYL-1-BROMO-1-DEOXY-BETA-D-GALACTOPYRANOSYL)FORMAMIDE;C-(2,3,4,6-TETRA-O-ACETYL-1-BROMO-1-DEOXY-SS-D-GALACTOPYRANOSYL)FORMAMIDE
    3. CAS NO:159895-07-5
    4. Molecular Formula: C15H20BrNO10
    5. Molecular Weight: 439.23254
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 159895-07-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: C-(2,3,4,6-TETRA-O-ACETYL-1-BROMO-1-DEOXY-BETA-D-GALACTOPYRANOSYL)FORMAMIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: C-(2,3,4,6-TETRA-O-ACETYL-1-BROMO-1-DEOXY-BETA-D-GALACTOPYRANOSYL)FORMAMIDE(159895-07-5)
    11. EPA Substance Registry System: C-(2,3,4,6-TETRA-O-ACETYL-1-BROMO-1-DEOXY-BETA-D-GALACTOPYRANOSYL)FORMAMIDE(159895-07-5)
  • 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: 159895-07-5(Hazardous Substances Data)

159895-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159895-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,8,9 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 159895-07:
(8*1)+(7*5)+(6*9)+(5*8)+(4*9)+(3*5)+(2*0)+(1*7)=195
195 % 10 = 5
So 159895-07-5 is a valid CAS Registry Number.

159895-07-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name C-(2,3,4,6-TETRA-O-ACETYL-1-BROMO-1-DEOXY-β-D-GALACTOPYRANOSYL)FORMAMIDE

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:159895-07-5 SDS

159895-07-5Relevant articles and documents

Anomeric α-azido acid (2-azido-2-deoxy-hept-2-ulopyranosonic acid) derivatives en route to peptides incorporating sugar amino acids

Czifrak, Katalin,Szilagyi, Peter,Somsak, Laszlo

, p. 127 - 141 (2007/10/03)

Per-O-acylated 2,6-anhydro-aldoheptonic acids of d-glycero-d-gulo and d-glycero-l-manno configuration obtained by nitrosation of the corresponding aldonamides were transformed into methyl-, tert-butyl-, 2,2,2-trichloroethyl-, and pentachlorophenyl esters,

Radical-mediated bromination of carbohydrate derivatives: Searching for alternative reaction conditions without carbon tetrachloride

Czifrák, Katalin,Somsák, László

, p. 8849 - 8852 (2007/10/03)

KBrO3-Na2S2O4 in CH2Cl2-H2O or PhCF3-H2O biphasic solvent systems was applied to the bromination of several monosaccharide derivatives having capto-datively

A straightforward route to hydantocidin analogues with pyranose ring structure

Osz, Erzsebet,Sos, Erzsebet,Somsak, Laszlo,Szilagyi, Laszlo,Dinya, Zoltan

, p. 5813 - 5824 (2007/10/03)

Partial hydrolysis of the nitrile moiety in aeetylated 1-bromo-glycopyranosyl cyanides 1 and 9 mediated by TiCl4 gave C-(1-bromo-1-deoxy-glycopyranosyl) formamides 2 and 10 whose reaction either with AgOCN, AgSCN or KSCN in nitromethane resulted in the formation of glycopyranosylidene-spirohydantoins 3, 11 and 15 and -thiohydantoins 7 and 16. Zemplen-deacetylation gave the pyranoid epihydantocidin analogues 4 and 12, and thiohydantocidin analogues 8 and 17, respectively.

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