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1-(2-Methoxyphenyl)propane-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74702-94-6

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74702-94-6 Usage

Type of Drug

Central nervous system stimulant

Chemical Similarity

Similar to amphetamine

Psychoactive Effects

Increased alertness, energy, and euphoria

Addictiveness

Highly addictive

Health Consequences

Increased heart rate, elevated blood pressure, potentially fatal overdoses

Abuse

Commonly abused as a recreational drug and used illicitly for its stimulant effects

Legal Classification

Schedule II controlled substance in the United States

Reasons for Classification

High potential for abuse and addiction

Check Digit Verification of cas no

The CAS Registry Mumber 74702-94-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,0 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74702-94:
(7*7)+(6*4)+(5*7)+(4*0)+(3*2)+(2*9)+(1*4)=136
136 % 10 = 6
So 74702-94-6 is a valid CAS Registry Number.

74702-94-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methoxyphenyl)propan-2-amine

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:74702-94-6 SDS

74702-94-6Relevant academic research and scientific papers

NITROGEN-CONTAINING SATURATED HETEROCYCLIC COMPOUND

-

Paragraph 0344, (2016/08/29)

The present invention provides a compound represented by the following formula (I) or its pharmaceutically acceptable salt: [wherein, R1 represents optionally substituted C1-4 alkyl, n shows integer of 1 to 4, R2 represents optionally substituted C1-4 alkyl or hydrogen atom, R3 represents optionally substituted C1-4 alkyl, R4a, R4b, R4c, and R4d, similarly or differently, represent optionally substituted C6-14 aryl, optionally substituted C1-4 alkyl, or hydrogen atom and the like, A represents optionally substituted C6-14 aryl or optionally substituted 5 to 11 membered heteroaryl].

10A-AZALIDE COMPOUND HAVING 4-MEMBERED RING STRUCTURE

-

Page/Page column 37, (2011/04/14)

A 10a-azalide compound having a 4-membered ring structure crosslinked at the 10a- and 12-positions, which is represented by the formula (I), and is effective on even Haemophilus influenzae, or erythromycin resistant bacteria (e.g., resistant pneumococci and streptococci).

Organocerium reactions of benzamides and thiobenzamides: A direct synthesis of tertiary carbinamines

Calderwood, David J.,Davies, Roy V.,Rafferty, Paul,Twigger, Helen L.,Whelan, Helen M.

, p. 1241 - 1244 (2007/10/03)

A simple and efficient process has been developed for the direct conversion of benzamides and thiobenzamides into tertiary carbinamines. A synthesis of benzonitriles from simple benzamides and a thiobenzamide is also described.

Steroid derivatives for the treatment of prostatic hypertrophy their preparation and uses

-

, (2008/06/13)

The invention includes compounds of formula (I): STR1 in which R1 is hydrogen, alkyl, aryl-substituted alkyl or aromatic heterocyclic-substituted alkyl; R2 is aryl-substituted alkyl, aromatic heterocyclic-substituted alkyl or diarylamino; and R3 is carboxy or a group of formula --CONHSO2 R4 wherein R4 is alkyl; and pharmaceutically acceptable salts and esters of the compounds. The compounds have valuable 5α-reductase inhibitory activity and can thus be used for the treatment and prophylaxis of, inter alia, prostatic hypertrophy as well as other disorders arising from excess levels of 5α-dihydro-testosterone.

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