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78314-10-0

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78314-10-0 Usage

Physical state

Colorless liquid

Composition

Made up of two acetate groups attached to a 1,4-dibromobutane-2,3-diyl backbone

Usage

a. Reagent in organic synthesis
b. Cross-linking reagent in the synthesis of polymeric materials
c. Particularly used in the field of biocompatible materials and biomaterials
d. Preparation of various organic compounds
e. Studying chemical reactions

Appearance

Colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 78314-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,1 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78314-10:
(7*7)+(6*8)+(5*3)+(4*1)+(3*4)+(2*1)+(1*0)=130
130 % 10 = 0
So 78314-10-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H12Br2O4/c1-5(11)13-7(3-9)8(4-10)14-6(2)12/h7-8H,3-4H2,1-2H3

78314-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-acetyloxy-1,4-dibromobutan-2-yl) acetate

1.2 Other means of identification

Product number -
Other names 1,4-Dibromobutane-2,3-diyl diacetate

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:78314-10-0 SDS

78314-10-0Downstream Products

78314-10-0Relevant articles and documents

Expedious synthesis of polyhydroxylated selena and thia-heterocycles via Se and S-ring closure of α,ω-dibromoalditols

Benazza, Mohammed,Halila, Sami,Viot, Camille,Danquigny, Alain,Pierru, Christèle,Demailly, Gilles

, p. 2889 - 2895 (2007/10/03)

The selena and thiaanhydro alditols (with xylo, ribo, D-arabino, erythro, D,L-threo and D-manno configuration) were easily and expeditiously synthesized in good to excellent yields by reaction of selenure and sulfur ions as binucleophiles with α,ω-dibromo

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