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Ethanone, 2-amino-1-phenyl-, hydrobromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37394-53-9

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37394-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37394-53-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,3,9 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37394-53:
(7*3)+(6*7)+(5*3)+(4*9)+(3*4)+(2*5)+(1*3)=139
139 % 10 = 9
So 37394-53-9 is a valid CAS Registry Number.

37394-53-9SDS

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-amino-1-phenylethanone,hydrobromide

1.2 Other means of identification

Product number -
Other names Phenacylamine hydrobromide

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:37394-53-9 SDS

37394-53-9Relevant academic research and scientific papers

Azole derivatives as histamine H3 receptor antagonists, Part 2: C-C and C-S coupled heterocycles

Walter,Isensee,Kottke,Ligneau,Camelin,Schwartz,Stark

scheme or table, p. 5883 - 5886 (2010/11/18)

With a small series of compounds we demonstrated the variability in the core region of the human histamine H3 receptor (hH3R) antagonist structural blueprint by introducing polar azole groups (oxazole, oxadiazole, thiazole and triazole). Additional variations achieved by coupling different residues to the heterocyclic core structure led to further optimisation of in vitro receptor binding of the novel azole derivatives.

Investigations into the parallel synthesis of novel pyrrole-oxazole analogues of the insecticide pirate

Loughlin, Wendy A.,Henderson, Luke C.,Elson, Kathryn E.,Murphy, Michelle E.

, p. 1975 - 1980 (2007/10/03)

Investigations into the parallel synthesis of selected analogues of a structurally unique pyrrole-oxazole analogue of the pyrrole insecticide pirate, are reported. Acylaminoketone salts were obtained from ketobromides in moderate to high yields and excell

Synthesis of a novel pyrrole oxazole analogue of the insecticide pirate

Loughlin, Wendy A.,Murphy, Michelle E.,Elson, Kathryn E.,Henderson, Luke C.

, p. 227 - 232 (2007/10/03)

The pyrrole oxazole 4 is a novel analogue of the broad-spectrum insecticide and miticide pirate 2. The expedient synthesis of pyrrole oxazole 4 in six steps from pyrrole is reported using a synthetic route that could have potential for the solution-phase

SYNTHESIS OF LUMINOPHORIC DERIVATIVES OF PBD BASED ON 2,5-DIARYL SUBSTITUTED THIAZOLES AND OXAZOLES

Lhotak, Pavel,Kurfuerst, Antonin

, p. 2720 - 2728 (2007/10/02)

The Friedel-Crafts acylation of 2-(biphenyl-4-yl)-5-phenyl-1,3,4-oxadiazole (PBD) with hippuryl chloride has been used to prepare the derivative V which on cyclization with POCl3 or P4S10 gives the respective oxazole (or thiazole) derivative of PBD, XIa or XIb.The reaction of carboxylic acid II with 4-(ω-aminoacetyl)biphenyl in the presence of CDI gives N-acyl-α-aminoketone VII; the analogous compound VI has been prepared by acylating ω-aminoacetophenone with acyl chloride III.The cyclization of these compounds gives bifluorophores Xa - Xd.

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