Welcome to LookChem.com Sign In|Join Free

CAS

  • or

336628-67-2

Post Buying Request

336628-67-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

336628-67-2 Usage

Uses

2-Hydroxy-3-(trifluoromethyl)benzaldehyde can be used for pain treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 336628-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,6,6,2 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 336628-67:
(8*3)+(7*3)+(6*6)+(5*6)+(4*2)+(3*8)+(2*6)+(1*7)=162
162 % 10 = 2
So 336628-67-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H5F3O2/c9-8(10,11)6-3-1-2-5(4-12)7(6)13/h1-4,13H

336628-67-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H32858)  3-(Trifluoromethyl)salicylaldehyde, 98+%   

  • 336628-67-2

  • 250mg

  • 682.0CNY

  • Detail
  • Alfa Aesar

  • (H32858)  3-(Trifluoromethyl)salicylaldehyde, 98+%   

  • 336628-67-2

  • 1g

  • 1913.0CNY

  • Detail

336628-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-3-(trifluoromethyl)benzaldehyde

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-3-trifluoromethyl-benzaldehyde

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:336628-67-2 SDS

336628-67-2Downstream Products

336628-67-2Relevant articles and documents

Roles of phenol groups and auxiliary ligand of copper(II) complexes with tetradentate ligands in the aerobic oxidation of benzyl alcohol

Zhan, Guangli,Zhong, Wei,Wei, Zhenhong,Liu, Zhenzhen,Liu, Xiaoming

, p. 8286 - 8297 (2017/07/10)

Herein, six copper(ii) complexes with multidentate ligands, [Cu(HL1)(OAc)(HOAc)] (1), [Cu(HL2)(OAc)] (2), [Cu(HL3)(OAc)] (3), [CuL4(OAc)] (4), [Cu(HL2)Cl] (5), and [Cu(HL3)Cl] (6) {H2L1 = [bis(3-tert-butyl-2-hydroxybenzyl)](2-pyridylmethyl)amine, H2L2 = [(3-tert-butyl-2-hydoxybenzyl)(3-trifluoromethyl-2-hydroxybenzyl) (2-pyridylmethyl)]amine, H2L3 = [bis(3-trifluoromethyl-2-hydroxybenzyl)] (2-pyridylmethyl)amine, and HL4 = [bis(2-pyridylmethyl)] (3-tert-butyl-2-hydroxybenzyl)amine}, are reported. The complexes were characterized by UV-vis spectroscopy, high-resolution mass spectrometry, X-ray single-crystal diffraction analysis and electrochemistry. These copper(ii) complexes have been investigated as catalysts for the aerobic oxidation of benzyl alcohol to benzaldehyde mediated by TEMPO (2,2,6,6-tetramethylpiperidinyl-1-oxyl) radical in water at ambient temperature. Mechanistic investigations have revealed that the phenolate/phenol is involved in the intramolecular proton transfer with a bound substrate in catalysis. Hence, the presence of the trifluoromethyl group on the phenol ring significantly affects the catalysis process since the substituent affects the acidity of phenol, and subsequently, the intramolecular proton transfer from the bound substrate. During catalysis, the dissociation of the auxiliary ligand (Cl- or OAc-) occurred in the SN1 pathway, and it is necessary for the substrate to bind. To complete the catalytic cycle, the cleaved auxiliary ligand rebinds to the metal center to regenerate the catalyst.

GLUCOSYLCERAMIDE SYNTHASE INHIBITORS FOR THE TREATMENT OF DISEASES

-

Paragraph 0001035, (2015/04/15)

Described herein are compounds of Formula I, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or conditions associated with the enzyme glucosylceramide synthase (GCS).

Highly enantioselective henry reactions in water catalyzed by a copper tertiary amine complex and applied in the synthesis of (S)-N-trans-feruloyl octopamine

Lai, Guoyin,Guo, Fengfeng,Zheng, Yueqin,Fang, Yang,Song, Haigang,Xu, Kun,Wang, Sujing,Zha, Zhenggen,Wang, Zhiyong

, p. 1114 - 1117 (2011/03/21)

It's in the water! A new copper tertiary amine complex was prepared and applied in asymmetric Henry reactions in water and in the short synthesis of (S)-N-trans-feruloyl octopamine. This catalytic system provided an approach to the enantioselective Henry reaction of aldehydes with hydroxyl substituents (see graphic).

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 336628-67-2