39861-30-8

Basic information

• Product Name: 2-chloro-1-methyl-2-phenyl-ethylamine; hydrochloride
• Synonyms: 2-chloro-1-methyl-2-phenyl-ethylamine; hydrochloride
• CAS NO: 39861-30-8
• Molecular Weight: 206.115
• Mol File: 39861-30-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-chloro-1-methyl-2-phenyl-ethylamine; hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-1-methyl-2-phenyl-ethylamine; hydrochloride(39861-30-8)
• EPA Substance Registry System: 2-chloro-1-methyl-2-phenyl-ethylamine; hydrochloride(39861-30-8)

Safety Data

• Hazardous Substances Data: 39861-30-8(Hazardous Substances Data)

Upstream product

• 38222-77-4 trans-2,5-diphenyl-4-methyl-1,3-oxazoline 
• 38222-78-5 threo-1-benzoyloxy-1-phenyl-2-propylammonium chloride 
• 4380-71-6 erythro-2-benzoylamino-1-phenylpropan-1-ol 
• 154-41-6 threo-1-phenyl-1-hydroxy-2-propylammonium chloride 
• 154-41-6 erythro-1-phenyl-1-hydroxy-2-propylammonium chloride 
• 3198-15-0 (1R,2S)-(-)-norephedrine hydrochloride 

Downstream Products

• 802564-55-2 2-(4-methoxy-phenyl)-1-methyl-2-phenyl-ethylamine 
• 802259-63-8 1-Phenyl-1-(4-methyl-phenyl)-2-amino-propan 
• 3139-55-7 1,1-diphenylisopropylamine 
• 78393-88-1 erythro-1-chloro-1-phenyl-2-isothiocyanatopropane 
• 78393-88-1 threo-1-chloro-1-phenyl-2-isothiocyanatopropane 
• 78373-96-3 cis-5-phenyl-2-methoxy-4-methyl-1,3-thiazoline 
• 78374-02-4 cis-2-diethylamino-5-phenyl-4-methyl-1,3-thiazoline 
• 78374-00-2 cis-5-phenyl-2-phenylamino-4-methyl-1,3-thiazoline 
• 1630-31-5 cis-5-phenyl-4-methyl-1,3-thiazolidine-2-thione 
• 2706-50-5 amphetamine hydrochloride 
• 78374-00-2 trans-5-phenyl-2-phenylamino-4-methyl-1,3-thiazoline 
• 78374-02-4 trans-2-diethylamino-5-phenyl-4-methyl-1,3-thiazoline 
• 78373-96-3 trans-5-phenyl-2-methoxy-4-methyl-1,3-thiazoline 
• 1630-31-5 trans-5-phenyl-4-methyl-1,3-thiazolidine-2-thione 

Relevant articles and documents

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STEREOCHEMICAL COURSE OF THE REACTION OF 2-HALOETHYL ISOTHIOCYANATES WITH NUCLEOPHILES. sTEREOSPECIFIC ROUTE TO 4,5-DISUBSTITUTED Δ2-THIAZOLINES AND THIAZOLIDINE-2-THIONES

Diastereoisomeric 1-chloro-1-phenyl-2-isothiocyanatopropanes have been prepared.They reacted stereospecifically with CH3ONa, diethylamine, aniline and NaSH to give pure cis or trans-4,5-disubstituted Δ2-thiazolines and thiazolidine-2-thiones whose configuration was determined using the nuclear Overhauser effect.The preponderant conformation of diastereoisomeric 1-chloro-1-phenyl-2-isothiocyanatopropanes was estimated on the basis of coupling constants of vicinal protons.