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Heptyl, also known as heptyl group or heptyl radical, is an alkyl group consisting of seven carbon atoms (C7H15) derived from heptane. It is a branched or straight-chain hydrocarbon and is commonly used as a substituent in various organic compounds. Heptyl can be found in different isomers, such as n-heptyl, 2-methylhexyl, 3-methylhexyl, and 2,2-dimethylpentyl, among others. This group is utilized in the synthesis of various chemicals, pharmaceuticals, and fragrances, and plays a significant role in the chemical industry due to its versatile properties and applications.

3356-67-0

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3356-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3356-67-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3356-67:
(6*3)+(5*3)+(4*5)+(3*6)+(2*6)+(1*7)=90
90 % 10 = 0
So 3356-67-0 is a valid CAS Registry Number.

3356-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name heptane

1.2 Other means of identification

Product number -
Other names heptyl

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:3356-67-0 SDS

3356-67-0Upstream product

3356-67-0Downstream Products

3356-67-0Relevant academic research and scientific papers

ON THE REMOVAL OF METALLIC MIRRORS BY FREE RADICALS.

Rice,Tweedell

, p. 995 - 997 (2007/10/02)

Large radicals can be formed by passing chlorinated organic compounds at pressures of a few mm. , through a furnace containing a pellet of sodium and heated to 350-400 degree C. It is found that the only radicals that will remove metallic mirrors (of tellurium or antimony, etc. , previously deposited beyond the furnace) are those that can decompose into methyl or ethyl radicals plus an unsaturated molecule, without undergoing any transmigration of atoms. The authors also found, especially in the case of larger monochlorinated molecules, that there was some decomposition, approximately half, even in the absence of metallic sodium.

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