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18113-04-7

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18113-04-7 Usage

Chemical Properties

Yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 18113-04-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,1 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18113-04:
(7*1)+(6*8)+(5*1)+(4*1)+(3*3)+(2*0)+(1*4)=77
77 % 10 = 7
So 18113-04-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H7ClO2/c1-10-5-2-3-6(8)7(9)4-5/h2-4,9H,1H3

18113-04-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-5-methoxyphenol

1.2 Other means of identification

Product number -
Other names Phenol,2-chloro-5-methoxy

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:18113-04-7 SDS

18113-04-7Relevant articles and documents

NOVEL HETEROCYCLIC COMPOUNDS AS PESTICIDES

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Paragraph 0699-0702, (2020/03/09)

The invention relates to novel compounds of the formula (I) in which Z, Y, A1, A2, A3, A4, X, R7, R8 and R9 have the meanings mentioned above, and processes and intermediates for the preparation thereof, and their use for controlling animal pests, in particular insects.

Practical regioselective halogenation of vinylogous esters: Synthesis of differentiated mono-haloresorcinols and polyhalogenated resorcinols

Chen, Xiaohong,Liu, Xiaoguang,Martinez, Jenny S.,Mohr, Justin T.

, p. 3653 - 3665 (2016/06/06)

A practical and efficient method for the direct, regioselective conversion of vinylogous esters to haloresorcinols is reported. Control of the reaction conditions enables synthesis of either the 4- or 6-haloresorcinol isomers from a common precursor with excellent regiocontrol and high yield. The generality and functional group tolerance of this novel protocol is demonstrated. The utility of this methodology to access polyhaloresorcinols is also reported. These methods create useful functionalized building blocks for further synthetic applications.

Pharmaceutically Active Pyrazine Derivatives

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Paragraph 0635, (2014/11/11)

The invention provides compounds which inhibit or modulate the activity of Chk-1 kinase and which are useful in the treatment of cancer. The compounds have the general formula (1): and salts, N-oxides and tautomers thereof, wherein m is 2, 3 or 4; n is 0

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