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(E)-2,2,4,6,6-Pentamethyl-4-heptene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27656-49-1

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27656-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27656-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,5 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27656-49:
(7*2)+(6*7)+(5*6)+(4*5)+(3*6)+(2*4)+(1*9)=141
141 % 10 = 1
So 27656-49-1 is a valid CAS Registry Number.

27656-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-2,2,4,6,6-pentamethyl-3-heptene

1.2 Other means of identification

Product number -
Other names trans-2,2,4,6,6-Pentamethyl-hept-3-en

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:27656-49-1 SDS

27656-49-1Relevant academic research and scientific papers

1-(2,2-Dimethylpropyl)-3,5-dimethylbenzene, an Unexpected Side Product

Weiss, Willy,Winkler, Matthias,Musso, Hans

, p. 4006 - 4013 (2007/10/02)

The title compound 4 is formed in fair yield in addition to the oligomers of isobutene during synthesis of 3-tert-butyl-2,4-pentanedione (2) from 2,4-pentanedione (1) with tert-butylalcohol and perchloric acid in nitromethane.Acid-catalyzed condensation of 1 with isooctene 5 is discovered to be responsible for the formation of 4.This reaction yields other meta-neopentyl-substituted benzene derivatives (19,20,21) with several β-diketones.

C-N, Si-N and P-N Bond Cleavage in Reactions of Phosphorus Pentafluoride with a Fluorophosphine and a Fluorophosphorane, Containing the N-Trimethylsilyl-N-tert-butyl Group

Roeschenthaler, Gerd-Volker,Storzer, Werner,Schmutzler, Reinhard

, p. 1125 - 1129 (2007/10/02)

PF5 reacts with Me3Si(But)NPF2(E) (E = lone electron pair or OC(CF3)2C(CF3)2O) to give products whose formation can be rationalised in terms of assuming the decomposition of the intermediates F4PN(But)PF2(E) into ButF and F3P=N-PF2(E).But, in the presence of PF5, trimerises to give a 1:1 mixture of tri-iso-butene isomers.During this reaction HF is formed, giving rise to additional Si-N and P-N bond cleavage reactions in which the compounds ButNHPF2, F3P(E), ButNH3(+)PF6(-) and NH4(+)PF6(-) are formed. - Key words: N-trimethylsilyl-N-tert-butylaminodifluorophosphine, 2,2-Difluoro-2(N-trimethylsilyl-N-tert-butylamino)-4,4,5,5-tetrakis(trifluoromethyl)-1,3,2λ5-dioxaphospholane, 1:1 Mixture of Tri-isobutene Isomers

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