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40750-71-8

1-(CHLORO-DIFLUORO-METHOXY)-4-NITRO-BENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 40750-71-8 Structure

  • Basic information

    1. Product Name: 1-(CHLORO-DIFLUORO-METHOXY)-4-NITRO-BENZENE
    2. Synonyms: 1-(CHLORO-DIFLUORO-METHOXY)-4-NITRO-BENZENE;4-NITRO-1-(CHLORODIFLUOROMETHOXY)BENZENE;4-(CHLORODIFLUOROMETHOXY)NITROBENZENE;4-(Chlorodifluoromethoxy)nitrobenzene 98%;4-(Chlorodifluoromethoxy)nitrobenzene98%
    3. CAS NO:40750-71-8
    4. Molecular Formula: C7H4ClF2NO3
    5. Molecular Weight: 223.56
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 40750-71-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 265.2 °C at 760 mmHg
    3. Flash Point: 114.2 °C
    4. Appearance: /
    5. Density: 1.514 g/cm3
    6. Vapor Pressure: 0.0152mmHg at 25°C
    7. Refractive Index: 1.516
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(CHLORO-DIFLUORO-METHOXY)-4-NITRO-BENZENE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(CHLORO-DIFLUORO-METHOXY)-4-NITRO-BENZENE(40750-71-8)
    12. EPA Substance Registry System: 1-(CHLORO-DIFLUORO-METHOXY)-4-NITRO-BENZENE(40750-71-8)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 20/21/22-36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 40750-71-8(Hazardous Substances Data)

40750-71-8 Usage

Uses

1-(Chlorodifluoromethoxy)-4-nitrobenzene

Check Digit Verification of cas no

The CAS Registry Mumber 40750-71-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,5 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40750-71:
(7*4)+(6*0)+(5*7)+(4*5)+(3*0)+(2*7)+(1*1)=98
98 % 10 = 8
So 40750-71-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H4ClF2NO3/c8-7(9,10)14-6-3-1-5(2-4-6)11(12)13/h1-4H

40750-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[chloro(difluoro)methoxy]-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names 4-difluorochloromethoxy-nitrobenzene

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:40750-71-8 SDS

40750-71-8Relevant articles and documents

A 4 - ( chlorine two fluorine methoxy ) method for preparing aniline

-

Paragraph 0017; 0030; 0031, (2018/02/04)

The invention relates to a preparation method for 4-(chlorodifluoromethoxy)aniline. The method includes: taking trichloromethoxybenzene as the raw material, employing hydrogen fluoride to conduct selective fluorination to obtain chlorodifluoromethoxybenze

Preparation of alkyl and aryl chlorodifluoromethyl ethers using BrF 3

Hagooly, Youlia,Sasson, Revital,Welch, Michael J.,Rozen, Shlomo

experimental part, p. 2875 - 2880 (2009/04/07)

Both alkyl and aryl chlorothioformates could readily be obtained from the corresponding alcohols and thiophosgene. These families of compounds were treated with BrF3 to form the corresponding alkyl and aryl chlorodifluoromethyl ethers in 60-85% yields. The method is suitable for constructing a variety of aliphatic as well as electron-deficient aromatic chlorodifluoromethyl ethers. The reactions proceed under mild conditions and short reaction times. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

Process for the preparation of aromatic compounds which contain perfluorinated side-chains bonded via a heteroatom

-

, (2008/06/13)

Aromatic compounds which contain perfluorinated side-chains bonded via a heteroatom are prepared by treating aromatic compounds, which contain side-chains which are perhalogenated, but only partially fluorinated, and bonded via heteroatom, with a catalyst capable of transferring halogen atoms.

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