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49823-06-5

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49823-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49823-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,2 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 49823-06:
(7*4)+(6*9)+(5*8)+(4*2)+(3*3)+(2*0)+(1*6)=145
145 % 10 = 5
So 49823-06-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H14Cl2N2O/c1-2-22-12-11-21-17(22)18(23,13-3-7-15(19)8-4-13)14-5-9-16(20)10-6-14/h2-12,23H,1H2

49823-06-5SDS

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 bis(4-chlorophenyl)-(1-ethenylimidazol-2-yl)methanol

1.2 Other means of identification

Product number -
Other names bis-(4-chloro-phenyl)-(1-vinyl-1H-imidazol-2-yl)-methanol

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:49823-06-5 SDS

49823-06-5Downstream Products

49823-06-5Relevant articles and documents

Analgesic imidazolemethanols

-

, (2008/06/13)

α,α-Diarylimidazole-2-methanols of the general formula STR1 wherein R1 -R10 are the same or different and each represents a hydrogen or halogen atom or a trifluoromethyl or tertiary butyl group, with at least one of said R1 -R10 being halogen, trifluoromethyl or tertiary butyl; R11 and R12 are the same or different and each represents a hydrogen atom, an alkyl group, a phenyl group or a halogen-or trifluoromethyl-substituted phenyl group; and R13 represents a hydrogen atom or a lower alkyl group, a lower alkoxymethyl group, a phenylalkyl group (optionally substituted in the phenyl moiety by one or more halogen atoms or alkyl or trifluoromethyl groups), an alkenyl group, a phenyl(lower)alkoxymethyl group (optionally substituted in the phenyl moiety by one or more halogen atoms or alkyl or trifluoromethyl groups) or a benzenesulfonyl group (in which the phenyl moiety is optionally substituted by one or more alkyl groups) are described. These compounds and their non-toxic acid addition salts have anorexient activity. Certain of these compounds have analgesic activity comparable to morphine but without its serious side effects. Processes for their manufacture and compositions for their use are described.

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