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1-(2,4-dichlorophenyl)butan-2-amine, also known as 2,4-dichloroamphetamine, is a chemical compound with the molecular formula C10H13Cl2N. It is classified as a substituted amphetamine and is structurally related to the recreational drug MDMA. 1-(2,4-dichlorophenyl)butan-2-aMine is not commonly encountered in scientific literature or in street drug formulations, and its pharmacological effects and potential toxicity are not well characterized. The parent compound amphetamine is known to act as a central nervous system stimulant, increasing the levels of neurotransmitters such as dopamine and norepinephrine in the brain. However, the specific effects and potential risks associated with 1-(2,4-dichlorophenyl)butan-2-amine have not been extensively studied, and caution should be exercised when handling or experimenting with 1-(2,4-dichlorophenyl)butan-2-aMine.

100428-40-8

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100428-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100428-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,2 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100428-40:
(8*1)+(7*0)+(6*0)+(5*4)+(4*2)+(3*8)+(2*4)+(1*0)=68
68 % 10 = 8
So 100428-40-8 is a valid CAS Registry Number.

100428-40-8SDS

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 6-[(tert-butyldiphenylsilyl)oxy]-2,4,8-tetradecatrien-1-ol

1.2 Other means of identification

Product number -
Other names -

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:100428-40-8 SDS

100428-40-8Relevant academic research and scientific papers

The Total Synthesis of 12-HETE and 12,20-DiHETE

Leblanc, Yves,Fitzsimmons, Brian J.,Adams, Julian,Perez, Francoise,Rokach, Joshua

, p. 789 - 793 (2007/10/02)

The total syntheses of 12-HETE (1) in racemic form and of both enantiomers in optically pure form are reported.The synthesis of a metabolite of 12(S)-HETE, 12,20-diHETE (2), in optically pure form is also reported.

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