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1079-44-3

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1079-44-3 Usage

Uses

[2-(2,5-Dimethyl-1H-indol-3-yl)ethyl]amine is used as a reactant in the total synthesis of (+)-minfiensine and related compounds via asymmetric cascade cyclization.

Check Digit Verification of cas no

The CAS Registry Mumber 1079-44-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1079-44:
(6*1)+(5*0)+(4*7)+(3*9)+(2*4)+(1*4)=73
73 % 10 = 3
So 1079-44-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2/c1-8-3-4-12-11(7-8)10(5-6-13)9(2)14-12/h3-4,7,14H,5-6,13H2,1-2H3

1079-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,5-dimethyl-1H-indol-3-yl)ethanamine

1.2 Other means of identification

Product number -
Other names 2,5-Dimethyltryptamine

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:1079-44-3 SDS

1079-44-3Relevant articles and documents

-

Grandberg,Bobrova

, (1974)

-

Asymmetric fluorinative dearomatization of tryptamine derivatives

Liang, Xiao-Wei,Liu, Chuan,Zhang, Wei,You, Shu-Li

supporting information, p. 5531 - 5534 (2017/07/07)

An asymmetric fluorinative dearomatization reaction of tryptamine derivatives was developed by using a chiral anion phase transfer catalyst (PTC) system, and the preliminary results of the reaction mechanistic study were achieved. This method is characterized by a simple operation, facile introduction of a fluorine atom in a highly enantioselective manner and construction of two contiguous quaternary stereogenic centers.

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