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N-Benzyl-2-(1-pyrrolidinyl)ethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65875-38-9

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65875-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65875-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,7 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65875-38:
(7*6)+(6*5)+(5*8)+(4*7)+(3*5)+(2*3)+(1*8)=169
169 % 10 = 9
So 65875-38-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H20N2/c1-2-6-13(7-3-1)12-14-8-11-15-9-4-5-10-15/h1-3,6-7,14H,4-5,8-12H2

65875-38-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-2-pyrrolidin-1-ylethanamine

1.2 Other means of identification

Product number -
Other names N-benzyl-2-(pyrrolidin-1-yl)ethanamine

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:65875-38-9 SDS

65875-38-9Downstream Products

65875-38-9Relevant academic research and scientific papers

PYRAZOLO[1,5-a]PYRIMIDINECARBOXAMIDE DERIVATIVES FOR TREATING COGNITIVE IMPAIRMENT

-

Paragraph 0034, (2015/07/07)

Compounds of formula I and II: Formula (I) or Formula (II) inhibit the interaction between fibrinogen and amyloid-β and are useful for treating cognitive disorders such as memory impairment and Alzheimer's disease.

SYNTHESIS AND REDUCTION OF N-SUBSTITUTED AMIDES OF 2-OXO-1-PYRROLIDINEACETIC ACID

Malawska, Barbara,Gorczyca, Maria

, p. 811 - 818 (2007/10/02)

N-Substituted amides of 2-oxo-1-pyrrolidineacetic acid were obtained.Bis-amides were reduced with activated sodium borohydride.Depending on the time of the reaction, products of reduction of one or both amide grouping were obtained.Their structures were established by the elemental and spectral (IR, UV, 1H NMR, MS) analyses.

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