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Benzene, (2-butyl-3,3-dimethyl-1-cyclopropen-1-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109900-82-5

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109900-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109900-82-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,9,0 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 109900-82:
(8*1)+(7*0)+(6*9)+(5*9)+(4*0)+(3*0)+(2*8)+(1*2)=125
125 % 10 = 5
So 109900-82-5 is a valid CAS Registry Number.

109900-82-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-butyl-3,3-dimethylcyclopropen-1-yl)benzene

1.2 Other means of identification

Product number -
Other names 1-(3,3-dimethyl-2-phenylcyclopropen-1-yl)-1-butane

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:109900-82-5 SDS

109900-82-5Downstream Products

109900-82-5Relevant academic research and scientific papers

Photochemistry of Cyclopropene Derivatives. 34. Photocycloaddition Reactions of 2-Alkenyl-Substituted Cyclopropenes

Padwa, Albert,Krumpe, Keith E.,Terry, Lenny W.,Wannamaker, M. Woods

, p. 1635 - 1642 (2007/10/02)

The sensitized irradiation of 2-(4-pentenyl)-substituted cyclopropenes produces tricyclo1,3>octanes by means of novel intramolecular cycloaddition.In dramatic contrast to the photochemical results, thermolysis affords a product co

Photochemistry of Cyclopropene Derivatives. Intramolecular Hydrogen Transfer Reaction of Some 1-(Alkyl-substituted)cyclopropenes

Padwa, Albert,Chou, Chuen S.,Rosenthal, Robert J.,Terry, Lenny W.

, p. 4193 - 4201 (2007/10/02)

The photochemical behavior of a number of 1-(alkyl-substituted)cyclopropenes that contain a hydrogen atom in the γ or δ position of the side chain has been studied in mechanistic detail.The triplet state, generated by sensitization techniques, undergoes hydrogen atom abstraction by a mechanism analogous to the Norrish type II process of carbonyl compounds.The quantum yield for the triplet-state hydrogen transfer reaction decreased substantially with deuterium substitution.The value of the isotope effect (kH/kD ca. 3.0) correlated well with related results in the literature indicating an early transition state for hydrogen transfer.The high regioselectivity of hydrogen transfer can be attributed to the stereoelectronic requirements for abstraction as well as the fact that the resulting diradical produced allows for maximum delocalization of the radical centers.

NUCLEOPHILIC SUBSTITUTION REACTIONS OF 1-SULFONYL SUBSTITUTED CYCLOPROPENES WITH ALKYL LITHIUM REAGENTS

Padwa, Albert,Wannamaker, M. Woods

, p. 5817 - 5820 (2007/10/02)

Sulfonyl substituted cyclopropenes react with a variety of alkyl lithium reagents to give disubstituted cyclopropenes in good yield.

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