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Chloroformic acid 2-chloro-1-methylethyl ester, also known as 2-chloro-1-methylethyl chloroformate, is an organic compound with the chemical formula C4H7Cl3O2. It is a colorless liquid that is soluble in most organic solvents. This ester is synthesized by the reaction of chloroformic acid with 2-chloro-1-methylethyl alcohol (also known as tert-butanol). It is used as a reagent in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. Due to its reactivity, it is important to handle Chloroformic acid 2-chloro-1-methylethyl ester with care, as it can be harmful if inhaled, ingested, or absorbed through the skin.

817-80-1

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817-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 817-80-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 817-80:
(5*8)+(4*1)+(3*7)+(2*8)+(1*0)=81
81 % 10 = 1
So 817-80-1 is a valid CAS Registry Number.

817-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloropropan-2-yl carbonochloridate

1.2 Other means of identification

Product number -
Other names 2-chloro-1-methylethyl chloroformate

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:817-80-1 SDS

817-80-1Relevant academic research and scientific papers

PROCESS FOR THE MANUFACTURING OF A POLYMER WITH URETHANE GROUPS

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Page/Page column 27-28, (2019/03/05)

Object of the invention is a process for the manufacturing of a polymer with urethane groups, wherein in a first alternative A)a five-membered cyclic monothiocarbonate B)a compound with at least two amino groups, selected from primary or secondary amino groups, and C)a compound which at least two functional groups that react with a group -SH or, in case of a carbon-carbon triple bond as functional group that react with a group -SH, a compound with at least one carbon-carbon triple bond are reacted or wherein in a second alternative A)a five-membered cyclic monothiocarbonate and D)a compound with at least one primary or secondary amino group and at least one functional group that reacts with a group -SH.

PROCESS FOR THE MANUFACTURING OF A POLYMER WITH URETHANE GROUPS

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Page/Page column 31-33, (2019/03/05)

Process for the manufacturing of a polymer with urethane groups, wherein in a first alternative a compound A) with at least two five-membered cyclic monothiocarbonate groups and a compound B) with at least two amino groups, selected from primary or second

METHOD FOR THE PREPARATION OF THIOCARBONATES

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Page/Page column 21-22, (2019/03/05)

Process for the preparation of a compound with at least one five-membered cyclic monothiocar- bonate group wherein a) a compound with at least one epoxy group is used as starting material b) the compound is reacted with phosgene or an alkyl chloroformate

Imidazopyridine azolidinones

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, (2008/06/13)

PCT No. PCT/EP95/02954 Sec. 371 Date Jan. 28, 1997 Sec. 102(e) Date Jan. 28, 1997 PCT Filed Jul. 26, 1995 PCT Pub. No. WO96/03405 PCT Pub. Date Feb. 8, 1996Imidazopyridine-azolidinones are useful for treating or preventing amenable gastro-intestinal ailme

Reaction of Epoxides with Chlorocarbonylated Compounds Catalyzed by Hexaalkylguanidinium Chloride

Gros, P.,Perchec, P. Le,Senet, J. P.

, p. 4925 - 4930 (2007/10/02)

Silica-supported guanidinium chloride (PBGSiCl) exhibits efficient chemo- and regiospecific catalytic activity in the ring opening of epoxides with various electrophiles.This reaction allows the preparation of β-chloro esters and β-chloro chloroformates in high yield under neutral conditions which offer product stability and ease of product isolation.

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