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77175-51-0

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77175-51-0 Usage

Metabolic pathway

When male rabbits are administered croconazole by intravenous injection, as many as 16 metabolites are excreted in the urine and 13 metabolites are identified. The biotransformation reaction of croconazole includes ring hydroxylation, O-dechlorobenzylation, and the loss of the imidazole ring.

Check Digit Verification of cas no

The CAS Registry Mumber 77175-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,7 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77175-51:
(7*7)+(6*7)+(5*1)+(4*7)+(3*5)+(2*5)+(1*1)=150
150 % 10 = 0
So 77175-51-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H15ClN2O/c1-14(21-10-9-20-13-21)17-7-2-3-8-18(17)22-12-15-5-4-6-16(19)11-15/h2-11,13H,1,12H2

77175-51-0SDS

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 CROCONAZOLE

1.2 Other means of identification

Product number -
Other names 1-[1-(2-(3-chlorobenzyloxy)phenyl)vinyl]imidazole

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:77175-51-0 SDS

77175-51-0Downstream Products

77175-51-0Relevant articles and documents

Synthesis and Antifungal Activity of New 1-Vinylimidazoles

Ogata, Masaru,Matsumoto, Hiroshi,Shimizu, Sumio,Kida, Shiro,Shiro, Motoo,Tawara, Katsuya

, p. 1348 - 1354 (2007/10/02)

Carbonyl compounds I were subjected to an imidazole transfer reaction with N,N'-sulfinyldiimidazole or N,N'-carbonyldiimidazole to obtain the diimidazole II and the monoimidazole III.Various 1-vinylimidazoles IV, derived from o-hydroxyacetophenones by imi

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