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Cyclohexanol, 2-chloro-1-ethynyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100313-83-5

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100313-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100313-83-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,1 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100313-83:
(8*1)+(7*0)+(6*0)+(5*3)+(4*1)+(3*3)+(2*8)+(1*3)=55
55 % 10 = 5
So 100313-83-5 is a valid CAS Registry Number.

100313-83-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-ethynylcyclohexanol

1.2 Other means of identification

Product number -
Other names 2-Chloro-1-ethynyl-cyclohexanol

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:100313-83-5 SDS

100313-83-5Relevant academic research and scientific papers

Halogen-Substituted Allenyl Ketones through Ring Opening of Nonstrained Cycloalkanols

Wu, Penglin,Ma, Shengming

supporting information, p. 2533 - 2537 (2021/04/13)

An efficient synthesis of halogen-substituted allenyl ketones via Ag-catalyzed oxidative ring opening of allenyl cyclic alcohols under mild reaction conditions has been achieved. The reaction features a wide substrate scope and excellent regioselectivity. The synthetic potential of the products has been demonstrated by their conversion to stereodefined alkenes and heterocyclic compounds.

Preparation of substituted transition-metal (η1-propargyl complexes and their [3+2] cycloaddition reactions with sulfur dioxide and disulfur monoxide. Transition-metal - Carbon bond cleaving reactions of the cycloadducts which yield oxathiolene oxides and dithiolene oxides

Scott, Elizabeth E.,Donnelly, Erling T.,Welker, Mark E.

, p. 67 - 76 (2007/10/03)

The preparations of several new cyclopentadienyl iron dicarbonyl η1-2-alkynyl complexes are reported. Their [3+2] cycloaddition reactions with sulfur dioxide and disulfur monoxide yielded transition-metal substituted 1,2-oxathiolene-2-oxides and 1,2-dithiolene-1-oxides, respectively. The transition-metal was cleaved from the oxathiolene-oxide and dithiolene-oxide containing complexes to produce new sulfur heterocycles.

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