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Benzenamine, N-[1-(2-propenyl)-3-butenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21855-35-6

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21855-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21855-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,5 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21855-35:
(7*2)+(6*1)+(5*8)+(4*5)+(3*5)+(2*3)+(1*5)=106
106 % 10 = 6
So 21855-35-6 is a valid CAS Registry Number.

21855-35-6SDS

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 N-hepta-1,6-dien-4-ylaniline

1.2 Other means of identification

Product number -
Other names 4-Anilino-hepta-1,6-dien

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:21855-35-6 SDS

21855-35-6Relevant academic research and scientific papers

Preparation of dihomoallylic secondary amines through samarium mediated allylation of oximes

Fan, Xuesen,Zhang, Yongmin

, p. 5475 - 5478 (2002)

The addition of allylsamarium bromide to oximes derived from aromatic aldehydes and methyl aryl ketones was studied and the dihomoallylic secondary amines were obtained in moderate to high yields under mild conditions.

Dimethylzinc-Mediated Chlorolactamization of Homoallylic Amines with Chloroform

Nishida, Yuika,Ueda, Masafumi,Hayashi, Masataka,Takeda, Norihiko,Miyata, Okiko

supporting information, p. 22 - 25 (2016/01/26)

A novel chlorolactamization reaction of homoallylic amines has been developed. The treatment of homoallylic amines with dimethylzinc in chloroform led to the formation of the corresponding β-chlorolactams via the Prins-type cyclization of a carbamoyl chlo

Endo-selective enyne ring-closing metathesis promoted by stereogenic-at-W mono-pyrrolide complexes

Zhao, Yu,Hoveyda, Amir H.,Schrock, Richard R.

supporting information; experimental part, p. 784 - 787 (2011/05/05)

The utility of W-alkylidene complexes for enyne ring-closing metathesis is demonstrated in a direct comparison with Mo-based analogs. Tungsten complexes lead to less alkyne oligomerization and higher levels of endo-selectivity and enantioselectivity.

The synthesis of N-(1-allyl-3-butenyl)-N-aryl amines by addition of organosamarium reagents to formanilides

Li, Zhifang,Zhang, Yongmin

, p. 297 - 298 (2007/10/03)

N-(1-allyl-3-butenyl)-N-aryl amines have been prepared for the first time in good yield via the direct diallylation reaction of formanilides with an organosamarium reagent under mild conditions.

Synthesis of Homoallylamines by the Addition of Allylic Indium Reagents to Azomethines and Nitriles

Jin, Shun-Ji,Araki, Shuki,Butsugan, Yasuo

, p. 1528 - 1532 (2007/10/02)

Triallyldiindium trihalides and allylindate(1-)s reacted with N-benzylideneamines regioselectively at the C-3 carbon on the allyl group to give high yields of homoallylic secondary amines.Primary amines were obtained by the action of an excess of allylic

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