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6708-14-1

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6708-14-1 Usage

Hazard

Moderately toxic by ingestion and inhala- tion.

Safety Profile

Moderately toxic by ingestion andinhalation routes. When heated to decomposition it emitsacrid smoke and irritating vapors.

Check Digit Verification of cas no

The CAS Registry Mumber 6708-14-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,0 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6708-14:
(6*6)+(5*7)+(4*0)+(3*8)+(2*1)+(1*4)=101
101 % 10 = 1
So 6708-14-1 is a valid CAS Registry Number.

6708-14-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclobutylidenecyclobutane

1.2 Other means of identification

Product number -
Other names Cyclobutylidinecyclobutane

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:6708-14-1 SDS

6708-14-1Relevant articles and documents

Everett,Garratt

, p. 642 (1972)

Synthesis of Spiro[2.2]pentanes and Spiro[2.3]hexanes Employing the Me3Al/CH2I2 Reagent

Ramazanov, Ilfir R.,Kadikova, Rita N.,Zosim, Tat'yana P.,Dzhemilev, Usein M.,de Meijere, Armin

, p. 7060 - 7067 (2017/12/28)

Substituted alkylidenecyclopropanes reacted with 5 equivalents each of Me3Al and CH2I2 at room temperature in hexane to give 1-mono- and 1,1-disubstituted spiro[2.2]pentanes in high yields. Surprisingly, the same reaction

Synthesis of energetic compounds via the metathesis reaction of 4-methylenespiro[2,3]hexane

Kotov,Chernykh,Finkel'shtein,Strel'chik,Tyshchenko,Milovantseva

experimental part, p. 309 - 313 (2010/03/24)

Transformations of methylenespiro[2,3]hexane (MSH) on a heterogeneous rhenium-alumina metathesis (disproportionation) catalyst were studied. It was found that, owing to a significant difference in the stability of carbenic complexes of methylene and disubstituted carbenes, MSH undergoes isomerization to 4-methylspiro[2,3]hex-4-ene followed by their cometathesis yielding bis(spiro[2,3]hexylidene-4). The feasibility of selective cometathesis of MSH and dicyclobutylidene on the rhenium-alumina catalyst resulting in the formation of 4-cyclobutylidenespiro[2,3]hexane was shown.

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