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2-(3,4-DIMETHOXY-PHENYL)-PYRROLIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

367281-00-3

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367281-00-3 Usage

Uses

2-(3,4-Dimethoxyphenyl)pyrrolidine

Check Digit Verification of cas no

The CAS Registry Mumber 367281-00-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,7,2,8 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 367281-00:
(8*3)+(7*6)+(6*7)+(5*2)+(4*8)+(3*1)+(2*0)+(1*0)=153
153 % 10 = 3
So 367281-00-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO2/c1-14-11-6-5-9(8-12(11)15-2)10-4-3-7-13-10/h5-6,8,10,13H,3-4,7H2,1-2H3

367281-00-3SDS

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 2-(3,4-Dimethoxy-phenyl)-pyrrolidine

1.2 Other means of identification

Product number -
Other names 2-(3,4-dimethoxyphenyl)pyrrolidine

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:367281-00-3 SDS

367281-00-3Relevant academic research and scientific papers

Asymmetric synthesis of crispine A: Constructing tetrahydroisoquinoline scaffolds using pummerer cyclizations

Rotte, Sateesh Chandra Kumar,Chittiboyina, Amar G.,Khan, Ikhlas A.

, p. 6355 - 6360 (2013/10/21)

For the first time, a concise, linear and stereoselective synthesis of both enantiomers of the natural product crispine A has been achieved in six steps with an overall yield of ≥ 20 %, starting from commercially available veratraldehyde. Asymmetric Keck allylation and trifluoroacetic anhydride-mediated Pummerer cyclization were the key transformations used to construct the tetrahydroisoquinoline core structure. Copyright

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