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

1027338-45-9

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1027338-45-9 Usage

Also known as

Cyclopropylamphetamine

Classification

Psychoactive drug

Type

Substituted amphetamine

Chemical structure

Derivative of amphetamine

Modification

Cyclopropyl group attached to the phenyl ring

Unique properties

Chemical and pharmacological

Reason

Due to the cyclopropyl group attachment

Research status

Not widely studied or used

Believed effects

Stimulant and hallucinogen

Impact

Effects on cognition, mood, and perception

Interaction

Dopamine and norepinephrine receptors in the brain

Result

Increased brain activity and altered perception

Safety and therapeutic uses

Not well understood

Need

Further research to determine safety and potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 1027338-45-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,3,3 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1027338-45:
(9*1)+(8*0)+(7*2)+(6*7)+(5*3)+(4*3)+(3*8)+(2*4)+(1*5)=129
129 % 10 = 9
So 1027338-45-9 is a valid CAS Registry Number.

1027338-45-9Relevant academic research and scientific papers

Enantioselective C-H Functionalization-Addition Sequence Delivers Densely Substituted 3-Azabicyclo[3.1.0]hexanes

Pedroni, Julia,Cramer, Nicolai

, p. 12398 - 12401 (2017)

An enantioselective C-H functionalization route to perfluoroalkyl-containing 3-azabicyclo[3.1.0]hexanes is disclosed. A modular and bench-stable diazaphospholane ligand enables highly enantioselective Pd(0)-catalyzed cyclopropane C-H functionalization using trifluoroacetimidoyl chlorides as electrophilic partners. In turn, the resulting cyclic ketimine products react smoothly with a broad variety of nucleophiles in one-pot processes enabling the rapid and modular construction of heavily substituted pyrrolidines.

(ALPHA-SUBSTITUTED ARALKYLAMINO AND HETEROARYLALKYLAMINO) PYRIMIDINYL AND 1,3,5-TRIAZINYL BENZIMIDAZOLES, PHARMACEUTICAL COMPOSITIONS THEREOF, AND THEIR USE IN TREATING PROLIFERATIVE DISEASES

-

Page/Page column 80, (2012/10/08)

Provided herein are (alpha-substituted aralkylamino or heteroarylalkylamino) pyrimidinyl and 1,3,5-triazinyl benzimidazoles, e.g., a compound of Formula 1, and their pharmaceutical compositions, preparation, and use as agents or drugs for treating proliferative diseases

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