Welcome to LookChem.com Sign In|Join Free

CAS

  • or
1-MethoxyMethoxy-3-trifluoroMethyl-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

334018-79-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 334018-79-0 Structure
  • Basic information

    1. Product Name: 1-MethoxyMethoxy-3-trifluoroMethyl-benzene
    2. Synonyms: 1-MethoxyMethoxy-3-trifluoroMethyl-benzene
    3. CAS NO:334018-79-0
    4. Molecular Formula: C9H9F3O2
    5. Molecular Weight: 206.1617696
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 334018-79-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 210.6±40.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.214±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-MethoxyMethoxy-3-trifluoroMethyl-benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-MethoxyMethoxy-3-trifluoroMethyl-benzene(334018-79-0)
    11. EPA Substance Registry System: 1-MethoxyMethoxy-3-trifluoroMethyl-benzene(334018-79-0)
  • 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: 334018-79-0(Hazardous Substances Data)

334018-79-0 Usage

Uses

1-(Methoxymethoxy)-3-(trifluoromethyl)benzene

Check Digit Verification of cas no

The CAS Registry Mumber 334018-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,4,0,1 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 334018-79:
(8*3)+(7*3)+(6*4)+(5*0)+(4*1)+(3*8)+(2*7)+(1*9)=120
120 % 10 = 0
So 334018-79-0 is a valid CAS Registry Number.

334018-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(methoxymethoxy)-3-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names methoxymethyl ether of 3-trifluoro-methylphenol

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:334018-79-0 SDS

334018-79-0Relevant articles and documents

INHIBITORS OF VIRAL REPLICATION, THEIR PROCESS OF PREPARATION AND THEIR THERAPEUTICAL USES

-

Page/Page column 152-153, (2012/11/06)

The present invention relates to compounds, their use in the treatment or the prevention of viral disorders, including HIV.

Chiral zirconium catalysts using multidentate BINOL derivatives for catalytic enantioselective Mannich-type reactions; ligand optimization and approaches to elucidation of the catalyst structure

Ihori, Yoichi,Yamashita, Yasuhiro,Ishitani, Haruro,Kobayashi, Shu

, p. 15528 - 15535 (2007/10/03)

Catalytic enantioselective Mannich-type reactions of silicon enolates with aldimines were investigated using chiral zirconium catalysts prepared from Zr(OtBu)4, N-methylimidazole, and newly designed multidentate BINOL derivatives. Th

Fluorophenols and (trifluoromethyl)phenols as substrates of site-selective metalation reactions: To protect or not to protect

Marzi, Elena,Mongin, Florence,Spitaleri, Andrea,Schlosser, Manfred

, p. 2911 - 2915 (2007/10/03)

O-Methoxymethyl (MOM) protected fluorophenols can be cleanly metalated and subsequently be submitted to site-selective electrophilic substitution. The 2- and 4-isomers exhibit ambivalent reactivity: deprotonation occurs at the position adjacent to the oxygen when butyllithium is employed whereas the position adjacent to the fluorine is attacked by the superbasic mixture of butyllithium and potassium tert-butoxide (LIC-KOR). The MOM-protected (trifluoromethyl)-phenols react exclusively at oxygen-neighboring positions. The meta isomer provides another example of optional site selectivity, undergoing hydrogen/metal exchange at the 2-position with the LIC-KOR reagent and at the 6-position with sec-butyllithium. Unprotected (trifluoromethyl)phenols can also be ortho-metalated after O-deprotonation, although the products are formed in only moderate yields.

Synthesis of constrained arylpiperidines using intramolecular Heck or radical reactions

Morice, Christophe,Domostoj, Mathias,Briner, Karin,Mann, André,Suffert, Jean,Wermuth, Camille-Georges

, p. 6499 - 6502 (2007/10/03)

Two intramolecular routes were experimented to reach the hexahydrobenzofuro[2,3-c]pyridine platform: a Heck and a radical reaction. The radical route was applicable to all substrates, whereas the Heck route was of limited use. The key adducts were obtained via a Mitsunobu condensation between halogenated phenols and an allylic alcohol, the 3-hydroxy-tetrahydropyridine.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 334018-79-0