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4335-93-7

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4335-93-7 Usage

General Description

1H-Indole-3-ethanamine,1-methoxy-N,Ndimethyl- is a chemical compound that consists of an indole group with an attached 3-ethanamine moiety and a methoxy-N,Ndimethyl substitution. It is commonly referred to as 5-MeO-DMT and is a naturally occurring psychedelic compound found in certain plants and the venom of the Bufo alvarius toad. 5-MeO-DMT is known for its hallucinogenic and entheogenic effects, and it is used for spiritual and recreational purposes. It is considered a Schedule I controlled substance in the United States due to its psychoactive properties.

Check Digit Verification of cas no

The CAS Registry Mumber 4335-93-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,3 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4335-93:
(6*4)+(5*3)+(4*3)+(3*5)+(2*9)+(1*3)=87
87 % 10 = 7
So 4335-93-7 is a valid CAS Registry Number.

4335-93-7SDS

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 lespedamine

1.2 Other means of identification

Product number -
Other names Lespedamin

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:4335-93-7 SDS

4335-93-7Downstream Products

4335-93-7Relevant articles and documents

Lithiation of 1-alkoxyindole derivatives

Nakagawa, Kyoko,Kobayashi, Tetsuya,Kawasaki, Toshiya,Somei, Masanori

, p. 968 - 997 (2019/04/26)

Lithiation of 1-alkoxyindoles, 3-dimethylaminomethyl- and 3-dimethylaminoethyl-1-methoxyindole occurred regioselectively at the 2-position. The introduction of a sterically bulky group into the 2-position of 3-dimethylaminomethyl-1-methoxyindoles directed the lithiation to the 4-position.

SIMPLE SYNTHESES OF LESPEDAMINE AND 5-BROMO-N,N-DIMETHYLTRYPTAMINE BASED ON 1-HYDROXYINDOLE CHEMISTRY

Somei, Masanori,Kobayashi, Kensuke,Tanii, Keiko,Mochizuki, Toshihiko,Kawada, Yumiko,Fukui, Yoshikazu

, p. 119 - 122 (2007/10/02)

Various types of 1-hydroxyindoles were prepared for the first time.Through methylation or acid catalyzed nucleophilic bromination of N,N-dimethyl-1-hydroxytryptamine, simple syntheses of lespedamine and 5-bromo-N,N-dimethyltryptamine were achieved, respectively.

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