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38461-17-5

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38461-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38461-17-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,6 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 38461-17:
(7*3)+(6*8)+(5*4)+(4*6)+(3*1)+(2*1)+(1*7)=125
125 % 10 = 5
So 38461-17-5 is a valid CAS Registry Number.

38461-17-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethylidenecyclohexene

1.2 Other means of identification

Product number -
Other names WTQHNWLXESYFAM-UHFFFAOYSA

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:38461-17-5 SDS

38461-17-5Relevant articles and documents

Intramolecular Cycloaddition Reactions of Dienyne Ethers. The Synthesis of Bridgehead Dienes and Their Thermal Rearrangements

Shea, K. J.,Burke, L. D.

, p. 318 - 327 (2007/10/02)

The type 2 intramolecular Diels-Alder cycloaddition of dienyne ethers 13-16, 18, 19, and 22-25 have been surveyed in both gas and solution phase.The dienyne ethers undergo cycloaddition to yield a novel class of bridgehead dienes of general structure 4.The stability and mode of thermal reactivity of the resulting bridgehead dienes varies as a function of the tether length.Bridgehead diene 37 has a half-life of 7 h at room temperature in dilute solution.The homologous bridgehead dienes 28 and 40, although reactive molecules, are considerably more stable than 37.At elevated temperatures, bridgehead diene 37 rearranges to propellanes 35 and 36, while bridgehead diene 41 undergoes dehydrogenation to yield metacyclophane 42.All intramolecular Diels-Alder reactions are found to give a single regioisomeric cycloadduct.

REGIOSELECTIVE Β-HYDRIDE TRANSFER IN REACTIONS OF ATE COMPLEXES OF BORON BICYCLIC AND CAGE COMPOUNDS. SYNTHESIS OF METHYLENECYCLOHEXANE DERIVATIVES

Bubnov, Yu. N.,Gurskii, M. E.,Grandberg, A. I.,Pershin, D. G.

, p. 1079 - 1092 (2007/10/02)

The reactions of bicyclic and cage boron containing ate complexes with AcCl have been studied, the key stage of which involves β-bridgehead hydride abstraction.The ate complexes of 7-substituted 3-methyl-3-borabicyclonon-6-ene were converted to the corresponding 5-methylene-3-alkylcyclohex-2(3)-en-1-ylmethyl(dialkyl)boranes 14 and 15.A synthetic application of the reaction is illustrated by conversion of compounds 14 and 15 to 3,5-dimethylene-1-R-cyclohexenes 16, particularly to 3,5-dimethylene-1-isopropenylcyclohexene (16c).The β-hydride transfer in ate complexes of 2-alkyl-1-boraadamantane and of 4-alkyl-3-borahomoadamantane occurs regioselectively, at the unsubstituted bridgehead, to give respectively, 2-alkyl-7-methylene-3-borabicyclononanes and 8-methylene-3-borabicyclodecanes.

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