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(+/-)-(1,3-dichloropropyl)cyclohexane is a chemical compound with the molecular formula C9H16Cl2. It is a chiral molecule, meaning it has two enantiomeric forms, (+) and (-), which are mirror images of each other. (+/-)-(1,3-dichloropropyl)cyclohexane consists of a cyclohexane ring with a 1,3-dichloropropyl group attached to it. The 1,3-dichloropropyl group contains two chlorine atoms attached to the first and third carbon atoms of a propane chain. This chemical is primarily used as a synthetic intermediate in the production of various pharmaceuticals and agrochemicals. Due to its potential applications and the presence of chlorine atoms, it is essential to handle (+/-)-(1,3-dichloropropyl)cyclohexane with care, as it may have environmental and health implications.

7015-06-7

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7015-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7015-06-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,1 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7015-06:
(6*7)+(5*0)+(4*1)+(3*5)+(2*0)+(1*6)=67
67 % 10 = 7
So 7015-06-7 is a valid CAS Registry Number.

7015-06-7Downstream Products

7015-06-7Relevant academic research and scientific papers

Chlorination of aliphatic primary alcohols via triphosgene-triethylamine activation

Ayala, Caitlan E.,Villalpando, Andres,Nguyen, Alex L.,McCandless, Gregory T.,Kartika, Rendy

supporting information; experimental part, p. 3676 - 3679 (2012/09/08)

Activation of primary aliphatic alcohols with triphosgene and triethylamine mixtures afforded either alkyl chloride or diethylcarbamate products, and the switch in selectivity appeared to be driven by sterics. The reaction conditions to achieve this highly useful transformation were unexceptionally mild and readily tolerated by a wide range of sensitive functionalities.

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