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150575-82-9

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150575-82-9 Usage

Description

Benzenemethanamine, 4-(1,1-dimethylethoxy)-α-methyl-, (S)is a specific enantiomer of a substituted amphetamine compound, commonly known as the "S-isomer" of 4-methylmethcathinone. It is a psychoactive stimulant and empathogen with a growing popularity as a recreational drug. However, it is associated with various health risks and adverse effects, necessitating careful handling and use in accordance with proper safety protocols due to its potential for abuse and health hazards.

Uses

Used in Recreational Drug Industry:
Benzenemethanamine, 4-(1,1-dimethylethoxy)-α-methyl-, (S)is used as a psychoactive substance for its stimulant and empathogenic effects, providing users with heightened energy, alertness, and feelings of empathy. However, its use in this industry is controversial and potentially dangerous due to the associated health risks and potential for abuse.

Check Digit Verification of cas no

The CAS Registry Mumber 150575-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,5,7 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 150575-82:
(8*1)+(7*5)+(6*0)+(5*5)+(4*7)+(3*5)+(2*8)+(1*2)=129
129 % 10 = 9
So 150575-82-9 is a valid CAS Registry Number.

150575-82-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzenemethanamine, 4-(1,1-dimethylethoxy)-a-methyl-, (S)-

1.2 Other means of identification

Product number -
Other names 1(S)-(4-tert-butoxyphenyl)-1-ethylamine

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:150575-82-9 SDS

150575-82-9Downstream Products

150575-82-9Relevant articles and documents

A novel constrained reduced-amide inhibitor of HIV-1 protease derived from the sequential incorporation of γ-turn mimetics into a model substrate

Newlander,Callahan,Moore,Tomaszek Jr.,Huffman

, p. 2321 - 2331 (2007/10/02)

C7 mimetics, designed to lock three amino acid residues of a peptide chain into a γ-turn conformation, were introduced sequentially between the P3 to P2' positions of a model HIV-1 protease substrate I (resulting in compou

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