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1-Chloro-3,3-dimethyl-2-methylidene-norbornane is a complex organic compound with the molecular formula C10H15Cl. It is a derivative of norbornane, a bicyclic hydrocarbon with a seven-membered ring fused to a two-membered ring. The compound features a chloro group (-Cl) at the 1-position, two methyl groups (-CH3) at the 3-position, and a methylidene group (-CH=) at the 2-position. This structure endows the compound with unique chemical properties and reactivity, making it a potential candidate for various applications in the chemical industry, such as in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its complex structure and potential applications, 1-chloro-3,3-dimethyl-2-methylidene-norbornane is a subject of interest for researchers in the field of organic chemistry.

4017-64-5

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4017-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4017-64-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,1 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4017-64:
(6*4)+(5*0)+(4*1)+(3*7)+(2*6)+(1*4)=65
65 % 10 = 5
So 4017-64-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H15Cl/c1-7-9(2,3)8-4-5-10(7,11)6-8/h8H,1,4-6H2,2-3H3

4017-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-2,2-dimethyl-3-methylidenebicyclo[2.2.1]heptane

1.2 Other means of identification

Product number -
Other names 1-chloro-3,3-dimethyl-2-methylene-norbornane

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

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More Details:4017-64-5 SDS

4017-64-5Relevant academic research and scientific papers

A mild synthesis of vinyl halides and gem-dihalides using triphenyl phosphite-halogen-based reagents

Spaggiari, Alberto,Vaccari, Daniele,Davoli, Paolo,Torre, Giovanni,Prati, Fabio

, p. 2216 - 2219 (2007/10/03)

A new application of (PhO)3P-halogen-based reagents to the synthesis of vinyl halides and gem-dihalides is described. Vinyl halides were prepared in good to excellent yields from enolizable ketones, whereas aldehydes afforded the corresponding gem-dihalides. The halogenation proceeded smoothly under mild conditions.

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