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[S,(+)]-α-Amino-α-phenylacetophenone is a chiral organic compound with the molecular formula C14H13NO. It is a derivative of acetophenone, featuring an amino group (-NH2) attached to the α-carbon, which is adjacent to the carbonyl group (C=O). The compound exhibits stereochemistry, with the (S,+) configuration indicating that the hydroxyl group and the phenyl ring are on the same side of the chiral center when viewed from the direction of the approaching hydrogen. [S,(+)]-α-Amino-α-phenylacetophenone is significant in the field of organic chemistry, particularly in the synthesis of pharmaceuticals and other chiral molecules, due to its unique structural properties and potential applications in asymmetric synthesis.

3723-23-7

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3723-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3723-23-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,2 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3723-23:
(6*3)+(5*7)+(4*2)+(3*3)+(2*2)+(1*3)=77
77 % 10 = 7
So 3723-23-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13H,15H2

3723-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1,2-diphenylethanone

1.2 Other means of identification

Product number -
Other names 2-amino-1,2-diphenyl-ethanone

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 -
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More Details:3723-23-7 SDS

3723-23-7Relevant academic research and scientific papers

Synthesis of some derivatives of 4,5-dihydrooxazoles

Piri, Farideh,Ghaforinia, Nastaran,Taghavi, Mohammad,Karimian, Ramin

experimental part, p. 1403 - 1406 (2012/04/10)

Benzaldehyds with sodium amide in the presence of thiourea in tetrahydro furan at room temperature gave various 2,4,5-triphenyl-4,5-dihydrooxazoles. The thiourea-catalyzed condensation of the benzaldehyde yielded 2-amino-1,2- diphenylethanone. Reduction of 2-amino-1,2-diphenylethanone was performed with hydride from Cannizzaro reaction to give 2-amino-1,2-diphenylethanols. The 4,5-dihydrooxazole ring formation of the 2-amino-1,2-diphenylethanol and benzamide gave the desired 4,5-dihydrooxazole.

Carbon Dioxide. A Reagent for the Protection of Nucleophilic Centers and the Simultaneous Activation for Electrophilic Attack. Part 4. The α-Substitution of (i) Benzyl Alcohol and (ii) Benzylamine

Katritzky, Alan R.,Fan, Wei-Qiang,Akutagawa, Kunihiko

, p. 415 - 418 (2007/10/02)

Benzyl alcohol is converted into a variety of α-substituted derivatives by a one-pot sequence involving lithiation of an intermediate hemicarbonate ester.Benzylamine is similarly converted by a one-pot sequence to α-substituted benzylamines: here an intermediate carbamate salt is involved.

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