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173838-41-0

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173838-41-0 Usage

Structure

Imidazole derivative with a butylamine side chain and a phenyl group attached to the imidazole ring

Usage

Intermediate in the synthesis of pharmaceuticals and other organic compounds

Potential applications

Development of new drugs due to structural versatility and ability to interact with biological systems

Industrial applications

Building block in the creation of new materials and compounds

Check Digit Verification of cas no

The CAS Registry Mumber 173838-41-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,8,3 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 173838-41:
(8*1)+(7*7)+(6*3)+(5*8)+(4*3)+(3*8)+(2*4)+(1*1)=160
160 % 10 = 0
So 173838-41-0 is a valid CAS Registry Number.

173838-41-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-phenylimidazol-1-yl)butan-1-amine

1.2 Other means of identification

Product number -
Other names 4-phenyl-1H-imidazole-1-butanamine

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:173838-41-0 SDS

173838-41-0Relevant articles and documents

Synthesis and antibacterial activity of HMR 3647 a new ketolide highly potent against erythromycin-resistant and susceptible pathogens

Denis, Alexis,Agouridas, Constantin,Auger, Jean-Michel,Benedetti, Yannick,Bonnefoy, Alain,Bretin, Francois,Chantot, Jean-Francois,Dussarat, Arlette,Fromentin, Claude,Gouin D'Ambrieres, Solange,Lachaud, Sylvette,Laurin, Patrick,Le Martret, Odile,Loyau, Veronique,Tessot, Nicole,Pejac, Jean-Marie,Perron, Sebastien

, p. 3075 - 3080 (2007/10/03)

In the search for new ketolides with improved activities against erythromycin-resistant S. pneumoniae and H. influenzae we synthesized a new 11,12 carbamate ketolide substituted by an imidazo-pyridyl side chain: HMR 3647. This compound demonstrated a potent activity against erythromycin susceptible and resistant pathogens, including penicillin G/erythromycin A-resistant S. pneumoniae and H. influenzae. In vivo, HMR 3647 displayed good pharmacokinetic parameters (Cmax = 2.9 μg/ml, bioavailability = 49%, AUC0-8 = 17.2 μg.h/l, t( 1/2 )= lh) and was shown to have a high therapeutic efficacy in mice infected by various respiratory pathogens, including multi-resistant S. pneumoniae and Gram negative bacteria such as H. influenzae. HMR 3647 appears to be a very promising agent for the treatment of respiratory infections and is currently in clinical trials.

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