15588-95-1 Suppliers

Recommended suppliersmore

This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

15588-95-1 Usage

Uses

Different sources of media describe the Uses of 15588-95-1 differently. You can refer to the following data:
1. 2,5-Dimethoxy-4-methylamphetamine (DOM, STP)
2. DOM is an amphetamine with dose-dependent psychotomimetic and hallucinogenic effects. It potently binds and activates serotonin 5-HT2 receptors (pA2 = 7.12). DOM is classified as a Schedule I compound in the United States. This product is intended for research and forensic purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 15588-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,8 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15588-95:
(7*1)+(6*5)+(5*5)+(4*8)+(3*8)+(2*9)+(1*5)=141
141 % 10 = 1
So 15588-95-1 is a valid CAS Registry Number.

InChI:InChI=1/C13H21NO2/c1-5-10-7-13(16-4)11(6-9(2)14)8-12(10)15-3/h7-9H,5-6,14H2,1-4H3

15588-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name	2,5-Dimethoxy-4-methylamphetamine

1.2 Other means of identification

Product number	-
Other names	2,5-dimethoxy-4-methylphenylisopropylamine

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:15588-95-1 SDS

15588-95-1Upstream product

15588-95-1Downstream Products

15588-95-1Relevant articles and documents

Stereospecific synthesis of amphetamines

Wagner, Jared M.,McElhinny Jr., Charles J.,Lewin, Anita H.,Carroll, F. Ivy

, p. 2119 - 2125 (2007/10/03)

Regioselective addition of aryl lithium to commercially available (S)-(+)-propylene oxide provides the corresponding (S)-aryl-2-propanol. The (R)-amphetamine is obtained by conversion of the alcohol to the tosylate followed by azide displacement and hydrogenation. Mitsunobu conversion of the alcohol to the (R)-bromide followed by azide displacement and hydrogenation affords the (S)-amphetamine.

CAS

15588-95-1