Welcome to LookChem.com Sign In|Join Free

CAS

  • or

174022-08-3

Post Buying Request

174022-08-3 Suppliers

Recommended suppliersmore

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

174022-08-3 Usage

General Description

(S)-(-)-2-(3,5-Di-tert-butylsalicylidene)-1,3-indandione, also known as (-)-DIK or (S)-(-)-2, is a chiral molecule that is commonly used as a ligand in asymmetric catalysis. It is a bright yellow solid that exhibits strong fluorescence when exposed to ultraviolet light. (S)-(-)-2-(3 5-DI-TERT-BUTYLSALICYLIDEN& is widely utilized in organic synthesis as a catalyst for various reactions, including asymmetric reduction, oxidation, and C-C bond formation. Additionally, it has found application in the preparation of chiral auxiliaries and pharmaceutical intermediates. Its unique molecular structure and versatile reactivity make it a valuable tool for achieving enantioselective transformations in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 174022-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,0,2 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 174022-08:
(8*1)+(7*7)+(6*4)+(5*0)+(4*2)+(3*2)+(2*0)+(1*8)=103
103 % 10 = 3
So 174022-08-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H35NO2/c1-19(2,3)15-10-14(12-22-17(13-23)21(7,8)9)18(24)16(11-15)20(4,5)6/h10-12,17,23-24H,13H2,1-9H3/b22-12+/t17-/m1/s1

174022-08-3SDS

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-[(E)-{[(2S)-1-Hydroxy-3,3-dimethyl-2-butanyl]imino}methyl]-4,6- bis(2-methyl-2-propanyl)phenol

1.2 Other means of identification

Product number -
Other names (S)-(-)-2-(3,5-di-tert-butylsalicilidenamino)-3,3-dimethyl-1-butanol

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:174022-08-3 SDS

174022-08-3Downstream Products

174022-08-3Relevant articles and documents

Enantioselective vanadium-catalyzed oxidation of 1,3-dithianes from aldehydes and ketones using β-amino alcohol derived schiff base ligands

Wu, Yinuo,Mao, Fei,Meng, Fanchao,Li, Xingshu

supporting information; experimental part, p. 1707 - 1712 (2011/10/01)

The asymmetric vanadium-catalyzed oxidation of 1,3-dithianes from aldehydes and ketones by β-amino alcohol-derived Schiff base ligands with two stereogenic centers was investigated. Using aqueous hydrogen peroxide as the oxidant and the Schiff base 3b as

Chiral binuclear copper(II) catalyzed nitroaldol reaction: scope and mechanism

Jammi, Suribabu,Saha, Prasenjit,Sanyashi, Sridhar,Sakthivel, Sekarpandi,Punniyamurthy, Tharmalingam

experimental part, p. 11724 - 11731 (2009/04/11)

Chiral binuclear copper(II) Schiff base complexes 4a-g have been prepared from aldehydes 1a,b, (S)-amino alcohols 2a-f, and Cu(OAc)2·1H2O in high yield. Their catalysis is studied for the addition of nitroalkanes to aldehydes at ambi

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 174022-08-3