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188428-48-0

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188428-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 188428-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,4,2 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 188428-48:
(8*1)+(7*8)+(6*8)+(5*4)+(4*2)+(3*8)+(2*4)+(1*8)=180
180 % 10 = 0
So 188428-48-0 is a valid CAS Registry Number.

188428-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name TRANS-2-FLUORO-CYCLOPROPANECARBOXYLIC ACID ETHYL ESTER

1.2 Other means of identification

Product number -
Other names TRANS-ETHYL 2-FLUOROCYCLOPROPANECARBOXYLATE

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:188428-48-0 SDS

188428-48-0Relevant articles and documents

Novel method for asymmetric synthesis of (1S,2S)-2-fluorocyclopropanecarboxylic acid under catalysis of chiral rhodium catalyst

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Paragraph 0124-0125; 0128-0129, (2019/12/02)

The invention provides a novel method for asymmetric synthesis of (1S, 2S)-2-fluorocyclopropanecarboxylic acid under catalysis of a chiral rhodium catalyst. The chiral rhodium catalyst not only can catalyze 1-fluoro-1-benzenesulfonyl ethylene and ethyl di

PROCESS FOR PREPARING HALOGENATED CYCLOPROPANE DERIVATIVES

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, (2008/06/13)

A process for preparing compounds represented by the following general formula (I) wherein X represents chlorine atom or other and R represents alkoxy group, amino group or other, which comprises the step of allowing a compound represented by the formula: CH2═CXF react with a compound represented by the formula: N2CHCOR in the presence of a catalyst containing a metal atom such as a transition metal of group 8 together with chiral carboxylic-type or amide-type ligands to preferentially obtain a stereoisomer of the compound of the general formula (I) wherein the stereochemical configuration at the 1-position is S-configuration

Selective dehalogenation process

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, (2008/06/13)

A compound represented by the following formula (1) or (3): STR1 is subjected to a catalytic hydrogenolysis reaction in the presence of a base and thus a compound represented by the following formula (2): STR2 wherein R represents a hydrogen atom or an al

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