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116355-65-8

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116355-65-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116355-65-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,3,5 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116355-65:
(8*1)+(7*1)+(6*6)+(5*3)+(4*5)+(3*5)+(2*6)+(1*5)=118
118 % 10 = 8
So 116355-65-8 is a valid CAS Registry Number.

116355-65-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(5-fluoro-2-nitrophenoxy)acetate

1.2 Other means of identification

Product number -
Other names methyl 5-fluoro-2-nitrophenoxyacetate

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:116355-65-8 SDS

116355-65-8Relevant articles and documents

Synthesis and biological evaluation of prodrugs for nitroreductase based 4-β-amino-4′-Demethylepipodophyllotoxin as potential anticancer agents

Deng, Wei,He, Dian,Wu, Zheng-Rong

, (2022/01/31)

A series of prodrugs for nitroreductase (NTR) based 4-β-amino-4′- Demethylepipodophyllotoxin as potential anticancer agents were synthesized, and their antiproliferative activities in vitro showed compounds 2b (IC50 = 0.77, 0.83 and 1.19 μM) an

Method for synthetizing 2-(5-fluorine-2-nitryl-phenoxyl) methyl acetate

-

Paragraph 0024; 0026; 0034-0037, (2018/04/01)

The invention discloses a method for synthetizing 2-(5-fluorine-2-nitryl-phenoxyl) methyl acetate. According to the method, 2,4-difluoronitrobenzene is used as raw materials; the 2-(5-fluorine-2-nitryl-phenoxyl) methyl acetate (a flumioxazin intermediate) is obtained through hydroxy substitution and etherification reaction. The synthesis method provided by the invention has the advantages that the 2,4-difluoronitrobenzene is used as raw materials; the price is low; the obtaining is easy, so that the production cost is reduced to a certain degree; the intermediate 1 directly reacts with methyl chloroacetate; the operation is simple; the raw materials can be repeatedly used, so that the production cost is reduced; through etherification reaction, byproducts of hydrochloric acid are recovered; no byproducts of sylvite are generated; environment-friendly and green effects are achieved; the aftertreatment operation is simple and convenient; in addition, the raw materials are cheap and can be easily obtained; the reaction condition are mild; the operation is simple and convenient; the popularization to scale production is favorably realized.

Herbicidal glutarimides

-

, (2008/06/13)

This invention relates to glutarimide compounds exhibiting herbicidal activity having the structure STR1 wherein A is carbonyl, thiocarbonyl or methylene, A1 is carbonyl or methylene, Q is O or (CH2)n where n is 0 or 1, D is CH or N and R, R1, R2, T, X, Y and Z are as defined within, compositions containing these compounds and methods of using these compounds as herbicides and algicides.

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