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Phenyl-N-(8-Quinolyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83848-82-2

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83848-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83848-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,4 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83848-82:
(7*8)+(6*3)+(5*8)+(4*4)+(3*8)+(2*8)+(1*2)=172
172 % 10 = 2
So 83848-82-2 is a valid CAS Registry Number.

83848-82-2SDS

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 phenyl N-quinolin-8-ylcarbamate

1.2 Other means of identification

Product number -
Other names quinolin-8-yl-carbamic acid phenyl ester

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:83848-82-2 SDS

83848-82-2Downstream Products

83848-82-2Relevant academic research and scientific papers

SULFONYLUREAS AND RELATED COMPOUNDS AND USE OF SAME

-

Page/Page column 181, (2016/09/15)

ABSTRACT The present invention provides for certain sulfonyl ureas and related compounds which have advantageous properties and show useful activity in the inhibition of activation of the NLRP3 inflammasome. Such compounds are useful in the treatment of a wide range of disorders in which the inflammation process, or more specifically the NLRP3 inflammasome, have been implicated as being a key factor.

HETEROARYL-SUBSTITUTED UREA MODULATORS OF FATTY ACID AMIDE HYDROLASE

-

Page/Page column 30, (2010/07/02)

Certain heteroaryl-substituted piperidinyl and piperazinyl urea compounds are described, which are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty acid amide hydrolase (FAAH) activity, such as anxiety, pain, inflammation, sleep disorders, eating disorders, insulin resistance, diabetes, osteoporosis, and movement disorders (e.g., multiple sclerosis).

Catalytic enantioselective additions of indoles to nitroalkenes

Ganesh, Madhu,Seidel, Daniel

supporting information; experimental part, p. 16464 - 16465 (2009/04/12)

A new design principle that provides access to more active thiourea catalysts is described. Highly enantioselective additions of indoles to nitroalkenes are reported using a new quinolinium thioamide catalyst. Copyright

Identification and biological evaluation of 4-(3-trifluoromethylpyridin-2- yl)piperazine-1-carboxylic acid (5-trifluoromethylpyridin-2-yl)amide, a high affinity TRPV1 (VR1) vanilloid receptor antagonist

Swanson, Devin M.,Dubin, Adrienne E.,Shah, Chandra,Nasser, Nadia,Chang, Leon,Dax, Scott L.,Jetter, Michele,Breitenbucher, J. Guy,Liu, Changlu,Mazur, Curt,Lord, Brian,Gonzales, Lisa,Hoey, Kenway,Rizzolio, Michele,Bogenstaetter, Michael,Codd, Ellen E.,Lee, Doo H.,Zhang, Sui-Po,Chaplan, Sandra R.,Carruthers, Nicholas I.

, p. 1857 - 1872 (2007/10/03)

High throughput screening using the recombinant human TRPV1 receptor was used to identify a series of pyridinylpiperazine ureas (3) as TRPV1 vanilloid receptor ligands. Exploration of the structure-activity relationships by parallel synthesis identified t

Synthesis and Reactions of Some Dihydro and Tetrahydro-4H-Imidazoquinoline Derivatives

Saari, Walfred S.,Halczenko, Wasyl,Freedman, Mark B.,Arison, Byron H.

, p. 837 - 840 (2007/10/02)

Reaction of phenyl N-(8-quinolyl)carbamate with sodium borohydride afforded 1,2-dihydro-4H-imidazoquinolin-2-one, 2a.The 5,6-double bond of 2a was functionalized by reaction with nitrosyl chloride to give the nitroolefin 4 and by reaction with h

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