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89766-09-6

89766-09-6

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89766-09-6 Usage

Synthesis Reference(s)

Synthetic Communications, 18, p. 1525, 1988 DOI: 10.1080/00397918808081309

Check Digit Verification of cas no

The CAS Registry Mumber 89766-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,6 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89766-09:
(7*8)+(6*9)+(5*7)+(4*6)+(3*6)+(2*0)+(1*9)=196
196 % 10 = 6
So 89766-09-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H9BrO3/c1-3-8-5(7)9-4(2)6/h4H,3H2,1-2H3

89766-09-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Bromoethyl ethyl carbonate

1.2 Other means of identification

Product number -
Other names 1-ethoxycarbonyloxyethyl bromide

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:89766-09-6 SDS

89766-09-6Relevant articles and documents

Cleavage of carbon-sulfur bonds in the synthesis of α-haloalkyl carbonates

Hatlelid, Jostein,Benneche, Tore,Undheim, Kjell

, p. 1041 - 1044 (2007/10/03)

α-Chloroalkyl and α-bromoalkyl carbonates have been prepared by cleavage of α-arylthioalkyl carbonates with sulfuryl chloride or bromine, respectively. The α-arylthioalkyl carbonates are prepared by reaction of the hemithioacetal 1 with chloroformates or by a destannylative tin-Pummerer rearrangement of α-stannyl sulfoxides. Acta Chemica Scandinavica 1996.

Androstane-17-beta-carboxylic-acid esters, process for their preparation and pharmaceutical compound containing them

-

, (2008/06/13)

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Preparation of 1'-ethoxycarbonyl-oxyethyl esters of penicillins

-

, (2008/06/13)

Process for the preparation of 1'-ethoxy carbonyloxy ethyl esters of penicillins, wherein a compound of the formula STR1 in which A is phenyl, phenoxy or 4-hydroxyphenyl, B is hydrogen, an amino group or a protected amino group and Z is hydrogen or a cation selected from the group of alkali metal, tri (lower alkyl ) ammonium and tetra (lower alkyl) ammonium, is reacted with 1-bromoethyl ethyl carbonate in an organic solvent and when B is a protected amino group the protecting group is split off to yield a primary amino group. There are also provided novel compounds of the formula STR2 in which Ph is phenyl and R is CH3 -- or C2 H5 --.

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