Welcome to LookChem.com Sign In|Join Free
  • or
3-Pentanone, 1-hydroxy-2,4,4-trimethyl-1-phenyl-, (1R,2R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

110012-45-8

Post Buying Request

110012-45-8 Suppliers

Recommended suppliers

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

110012-45-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110012-45-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,0,1 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 110012-45:
(8*1)+(7*1)+(6*0)+(5*0)+(4*1)+(3*2)+(2*4)+(1*5)=38
38 % 10 = 8
So 110012-45-8 is a valid CAS Registry Number.

110012-45-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2R)-1-hydroxy-2,4,4-trimethyl-1-phenyl-3-pentanone

1.2 Other means of identification

Product number -
Other names (R,R)-PhCH(OH)CHMeC(=O)CMe3

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:110012-45-8 SDS

110012-45-8Relevant academic research and scientific papers

Titanium tetraiodide-promoted reductive enolate formation of α-tosyloxy ketone derivatives and aldol reaction with aldehydes

Hachiya, Iwao,Inagaki, Takao,Ishihara, Yasuhisa,Shimizu, Makoto

experimental part, p. 419 - 421 (2011/05/16)

Titanium tetraiodide-promoted reductive enolate formation from α-tosyloxy ketone derivatives and subsequent aldol reaction of the resulting enolates with aldehydes gave β-hydroxy ketones.

Sml2-promoted reformatsky-type coupling reactions in exceptionally hindered contexts

Sparling, Brian A.,Moslin, Ryan M.,Jamison, Timothy F.

supporting information; experimental part, p. 1291 - 1294 (2009/04/08)

Highly substituted, very hindered enones were synthesized using a two-step procedure that utilizes a diiodosamarium-promoted Reformatsky-type coupling and dehydration using Martin sulfurane. Both α-chloro- and α-bromoketones were coupled with a variety of carbonyl nucleophiles to form the intermediate β-hydroxyketones, occurring with excellent diastereoselectivity, favoring the syn isomer (R1 = Me). This technique complements other methods and enables the preparation of enones outside of the scope of current olefination methodology.

From allylic alcohols to aldols through a new nickel-mediated tandem reaction: Synthetic and mechanistic studies

Cuperly, David,Petrignet, Julien,Crevisy, Christophe,Gree, Rene

, p. 3261 - 3274 (2008/09/18)

Nickel hydride type complexes have been successfully developed as catalysts for the tandem isomerization-aldolization reaction of allylic alcohols with aldehydes. Optimization of the reaction conditions has shown that a cocatalyst, such as MgBr2, has a very positive effect on the kinetics of the reaction and in the yields of aldols. Under such optimized conditions {[NiHCl(dppe)] + MgBr2 at 3-5 mol %)}, this reaction affords the aldols in good to excellent yields. It is a full-atom-economy-type reaction that occurs under mild conditions. Furthermore, it has a broad scope for the allylic alcohols and it is compatible with a wide range of aldehydes, including very bulky derivatives. The reaction is completely regioselective, but it exhibits a low stereoselectivity, except for allylic alcohols with a bulky substituent at the carbinol center. The use of chiral non-racemic catalysts was not successful, affording only racemic compounds. However, it was possible to use asymmetric synthesis for the preparation of optically active aldols. Various mechanistic studies have been performed using, for instance, a deuterated alcohol or a deuterated catalyst. They gave strong support to a mechanism involving first a transition-metal-mediated isomerization of the allylic alcohol into the free enol, followed by the addition of the latter intermediate onto the aldehyde in an "hydroxyl-carbonyl-ene" type reaction. These results confirm that allylic alcohols can be considered as new and useful partners in the development of the aldol reaction.

Chiral base-catalyzed aldol reaction of trimethoxysilyl enol ethers: Effect of water as an additive on stereoselectivities

Orito, Yuya,Hashimoto, Shunichi,Ishizuka, Tadao,Nakajima, Makoto

, p. 390 - 400 (2007/10/03)

An aldol reaction of trimethoxysilyl enol ether catalyzed by lithium binaphtholate is described. The aldol reaction of trimethoxysilyl enol ether derived from cyclohexanone under anhydrous conditions predominantly afforded the anti-aldol adduct with moder

BINAP/AgOTf/KF/18-crown-6 as new bifunctional catalysts for asymmetric Sakurai-Hosomi allylation and Mukaiyama aldol reaction

Wadamoto, Manabu,Ozasa, Nobuko,Yanagisawa, Akira,Yamamoto, Hisashi

, p. 5593 - 5601 (2007/10/03)

A catalytic amount of KF·18-crown-6 complex is effective as a soluble fluoride source to activate an asymmetric Sakurai-Hosomi allylation with BINAP and silver(I) triflate catalyst. The allylation of a variety of aromatic, α,β-unsaturated and aliphatic al

Ytterbium Trifluoromethanesulfonate Mediated Cross-Aldol Reaction between Ketones and Aldehydes

Fukuzawa, Shin-ichi,Tsuchimoto, Teruhisa,Kanai, Takeshi

, p. 2227 - 2232 (2007/10/02)

The cross-aldol reaction between a ketone and an aldehyde proceeded smoothly with threo diastereoselection favorably mediated by ytterbium trifluoromethanesulfonate and tertiary amine in diethyl ether or in dichloromethane.A ytterbium enolate was trapped

Enantioselective aldol reactions using homochiral lithium amides as non-covalently bound chiral auxiliaries

Landais,Ogay

, p. 541 - 544 (2007/10/02)

Syn and anti aldols have been prepared from ketones and esters respectively with relatively high enantiomeric excesses, using a homochiral lithium amide possessing two coordinating sites, as non-covalently bound chiral auxiliary.

Enolboration. 4. An Examination of the Effect of the Leaving Group (X) on the Stereoselective Enolboration of Ketones with Various R2BX/Et3N. New Reagents for the Selective Generation of either Z or E Enol Borinates from Representative Ketones

Brown, Herbert C.,Ganesan, Kumaraperumal,Dhar, Raj K.

, p. 147 - 153 (2007/10/02)

A smooth, rapid, quantitative and stereoselective enolboration of representative ketones to either Z or E enol borinates is achieved with many new R2BX/Et3N reagents.Representative B-X-9-BBN and Chx2BX reagents with various leaving groups, such as triflat

Enolboration. 5. An Examination of the Effects of Amine, Solvent, and Other Reaction Parameters on the Stereoselective Enolboration of Ketones with Various Chx2BX Reagents. An Optimized Procedure To Achieve the Stereoselective Synthesis of E Enol Borinate

Ganesan, Kumeraperumal,Brown, Herbert C.

, p. 7162 - 7169 (2007/10/02)

The effects of amine, solvent, concentration, temperature and other reaction parameters in controlling the enolate geometry have been systematically investigated in the present study.A 11B NMR study of the interaction of representative tertiary amines of

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 110012-45-8