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5-Quinolinecarboxylicacid,8-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74316-52-2 Structure
  • Basic information

    1. Product Name: 5-Quinolinecarboxylicacid,8-methyl-(9CI)
    2. Synonyms: 5-Quinolinecarboxylicacid,8-methyl-(9CI)
    3. CAS NO:74316-52-2
    4. Molecular Formula: C11H9NO2
    5. Molecular Weight: 187.19466
    6. EINECS: N/A
    7. Product Categories: QUINOLINE
    8. Mol File: 74316-52-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-Quinolinecarboxylicacid,8-methyl-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Quinolinecarboxylicacid,8-methyl-(9CI)(74316-52-2)
    11. EPA Substance Registry System: 5-Quinolinecarboxylicacid,8-methyl-(9CI)(74316-52-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 74316-52-2(Hazardous Substances Data)

74316-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74316-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,1 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74316-52:
(7*7)+(6*4)+(5*3)+(4*1)+(3*6)+(2*5)+(1*2)=122
122 % 10 = 2
So 74316-52-2 is a valid CAS Registry Number.

74316-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-methylquinoline-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 8-methylquinoline-5-carboxlic acid

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:74316-52-2 SDS

74316-52-2Relevant articles and documents

CXCR4-ANTAGONISTIC DRUGS COMPRISING NITROGEN-CONTAINING COMPOUND

-

Page/Page column 102, (2010/02/05)

To provide novel nitrogen-containing compounds having antagonism to CXCR4 and remedies for disease, such as rheumatism, cancer metastasis, etc., based on the CXCR4 antagonism. Nitrogen-containing compounds represented by the following general formula and

NITROGENOUS COMPOUNDS AND ANTIVIRAL DRUGS CONTAINING THE SAME

-

, (2008/06/13)

The present invention provides novel compounds having antiviral activities and antiviral drugs containing the compounds as the active ingredient. The compounds are shown by the following general formula (1), wherein typically A1 and A2 are each guanidine or a group of the general fomula (ia) ; A3 is a mono- or poly-cyclic heteroaromatic ring contining 1 or 2 heteroatoms ; B1 is a single bond or alkylene group; R1 is hydrogen or alkyl group; W is an alkylene having 2-3 carbons, a cycloalkylene having 5-10 carbons, aromatic ring having 6-10 carbons, or a heteroaromatic ring having 5-10 carbons; y is C(=O)-; x is -C(=O)-NH-; n1 is an integer of 1-2; n2 is an integer of 2-3; D is a substituent selected from among various groups.

SYNTHESIS AND BROMINATION OF 8-METHYLQUINOLINE-5-CARBOXYLIC ACID

Gracheva, I.N.,Tochilkin, A.I.

, p. 275 - 277 (2007/10/02)

8-Methylquinoline-5-carboxylic acid was obtained by the Skraup reaction from 3-amino-p-toluic acid or by hydrolysis of 5-cyano-8-methylquinoline.The latter was synthesized by the Rosemund-von Braun reaction from 5-bromo-8-methylquinoline, which was obtained by bromination of 8-methylquinoline in the presence of silver sulfate.Bromination in the side chain of 8-methylquinoline-5-carboxylic acid and its nitrile was studied.

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