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Benzenemethanamine, 3,4-dimethoxy-a-2-propenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83948-33-8

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83948-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83948-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,4 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83948-33:
(7*8)+(6*3)+(5*9)+(4*4)+(3*8)+(2*3)+(1*3)=168
168 % 10 = 8
So 83948-33-8 is a valid CAS Registry Number.

83948-33-8SDS

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 4-amino-4-(3,4-dimethoxyphenyl)-1-butene

1.2 Other means of identification

Product number -
Other names 1-(3,4-dimethoxyphenyl)but-3-enylamine

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:83948-33-8 SDS

83948-33-8Relevant academic research and scientific papers

Dual activation in asymmetric allylsilane addition to chiral N-acylhydrazones: Method development, mechanistic studies, and elaboration of homoallylic amine adducts

Friestad, Gregory K.,Korapala, Chandra Sekhar,Ding, Hui

, p. 281 - 289 (2007/10/03)

Chiral N-acylhydrazones derived from commercially available 4-benzyl-2-oxazolidinone provide a rigid, conformationally restricted template to impart facial selectivity in additions to C=N bonds. In the presence of indium(III) trifluoromethanesulfonate [In

A NEW SYNTHESIS OF PRIMARY AMINES FROM DIARYLIDENESULFAMIDES

Davis, Franklin A.,Giangiordano, Mark A.,Starner, William E.

, p. 3957 - 3960 (2007/10/02)

Addition of organometallic reagents to diarylidenesulfamides affords, after hydroylsis, primary amines illustrating the application of sulfamides as amino protecting groups.

Preparation of Primary Amines and 2-Azetidinones via N-Trimethylsilyl Imines

Hart, David J.,Kanai, Ken-ichi,Thomas, Dudley G.,Yang, Teng-Kuei

, p. 289 - 294 (2007/10/02)

Nonenolizable aldehydes react with lithium bis(trimethylsilyl)amide at ambient temperatures to afford solutions of N-trimethylsilyl aldimines.Treatment of these solutions with Grignard reagents or alkyllithiums followed by an aqueous workup gives primary amines in moderate to excellent yields.Treatment of N-trimethylsilyl aldimines with ester enolates provides an expedient route to 1-unsubstituted 2-azetidinones.

New Approach to Lythraceae Alkaloids: Total Synthesis of (+/-)-Vertaline

Hart, David J.,Kanai, Ken-ichi

, p. 1555 - 1560 (2007/10/02)

A new approach to Lythraceae alkaloids is described within the context of a total synthesis of (+/-)-vertaline (2).The use of N-silyl imines in the preparation of benzylic amines as well as a stereoselective bicycloannelation approach to the synthesis of quinolizidinones is discussed.

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