Welcome to LookChem.com Sign In|Join Free
  • or
Cyclohexanone, 2-([1,1'-biphenyl]-4-ylmethylene)-3-methyl-6-(1-methylethyl)-, (2E,3R,6R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144830-89-7

Post Buying Request

144830-89-7 Suppliers

Recommended suppliers

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

144830-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144830-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,8,3 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 144830-89:
(8*1)+(7*4)+(6*4)+(5*8)+(4*3)+(3*0)+(2*8)+(1*9)=137
137 % 10 = 7
So 144830-89-7 is a valid CAS Registry Number.

144830-89-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,4R)-2-(4-phenylbenzylidene)-p-menthan-3-one

1.2 Other means of identification

Product number -
Other names (3R,6R)-2-[1-Biphenyl-4-yl-meth-(E)-ylidene]-6-isopropyl-3-methyl-cyclohexanone

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:144830-89-7 SDS

144830-89-7Relevant academic research and scientific papers

Simple and effective protocol for Claisen-Schmidt condensation of hindered cyclic ketones with aromatic aldehydes

Vashchenko, Valeriy,Kutulya, Lidiya,Krivoshey, Alexander

, p. 2125 - 2134 (2008/03/28)

A simple and effective methodology for Claisen-Schmidt condensation of (-)-menthone and other hindered cyclic ketones with aromatic aldehydes under highly basic conditions using a polar aprotic solvent and a strong base (alkali metal hydroxide or an alkoxide) is described and discussed. Georg Thieme Verlag Stuttgart.

PHOTOCHEMICAL PROPERTIES OF CHIRAL 2-ARYLMETHYLENE-p-MENTHAN-3-ONES

Yarmolenko, S. N.,Chepeleva, L. V.,Kutulya, L. A.,Vashchenko, V. V.,Drushlyak, T. G.,Ponomarev, O. A.

, p. 127 - 136 (2007/10/03)

Quantitative aspects of E-Z photoisomerization of chiral (-)-2-arylidene-p-menthan-3-ones and model 2-benzylidenecyclohexanone and benzylidenepinacolone were studied.The photo-isomerization of 2-arylmethylenementhanones is not accompanied by inversion of the chiral center in the α-position to the carbonyl group; the quantum yields only slightly depend on the nature of the solvent and of the substituent in the aryl fragment.The quantum yield ratio for the direct and reverse photoreactions is much higher for cyclic α,β-unsaturated ketones than that for the related acyclic ketones, which is rationalized in terms of structural features of the E and Z isomers.Reasons for spectral differences between the E and Z forms are analyzed.

The Molecular Structure of Isomeric 2-Arylidene Derivatives of p-Menthanones and p-(4-Menthen)one and their Ability to Coil the Nematic Phase

Kutulya, R. A.,Yarmolenko, S. N.,Vashchenko, V. V.,Chepeleva, L. V.,Patsenker, L. D.,Ponomarev, O. A.

, p. 80 - 86 (2007/10/02)

The efficiency of inducing helical ordering in the nematic mesophase is markedly lower for the chiral Z isomers of 2-arylidene derivatives of diastereomeric p-menthanones and p-(4-menthen)one than for the corresponding E forms.The change in the sign of th

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 144830-89-7