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2-Butenedioic acid, 2-[2-(1-pyrrolidinyl)phenyl]-, dimethyl ester, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83466-98-2

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83466-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83466-98-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,6 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83466-98:
(7*8)+(6*3)+(5*4)+(4*6)+(3*6)+(2*9)+(1*8)=162
162 % 10 = 2
So 83466-98-2 is a valid CAS Registry Number.

83466-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-(2-pyrrolidin-1-ylphenyl)but-2-enedioate

1.2 Other means of identification

Product number -
Other names -

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:83466-98-2 SDS

83466-98-2Downstream Products

83466-98-2Relevant academic research and scientific papers

"tert-Amino Effect" in Heterocyclic Synthesis. Formation of N-Heterocycles by Ring-Closure Reactions of Substituted 2-Vinyl-N,N-dialkylanilines

Verboom, Willem,Reinhoudt, David N.,Visser, Richard,Harkema, Sybolt

, p. 269 - 276 (2007/10/02)

2-Vinyl-N,N-dialkylanilines react thermally in polar solvents and/or in the presence of Lewis acids via or hydrogen transfer followed by C-C bond formation to give heterotricyclic compounds.The reaction depends on the type of N,N-dialkylamino

1-Pyrrolidin-1-ylbuta-1,3-dienes as Potential 1,5-Dipoles; Synthesis of Pyrrolizines

Visser, Germ W.,Verboom, Willem,Benders, Piet H.,Reinhoudt, David N.

, p. 669 - 671 (2007/10/02)

Tautomerization of 1-pyrrolidin-1-ylbuta-1,3-dienes and (hetero)aromatic compounds formally containing this moiety, to the corresponding 1,5-dipoles by a concerted hydrogen shift is followed by a 1,5-electrocyclization to give pyrrolizine derivative

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