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65995-72-4

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65995-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65995-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,9 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65995-72:
(7*6)+(6*5)+(5*9)+(4*9)+(3*5)+(2*7)+(1*2)=184
184 % 10 = 4
So 65995-72-4 is a valid CAS Registry Number.

65995-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,5,5-tetramethyl-hexan-2-one

1.2 Other means of identification

Product number -
Other names 4,4,5,5-Tetramethyl-hexan-2-on

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:65995-72-4 SDS

65995-72-4Downstream Products

65995-72-4Relevant articles and documents

Preparation and reactivity of cyanocuprates containing alkylseleno and alkyltelluro groups as non-transferable ligands

Zinn, Fabiano K.,Ramos, Eduardo C.,Comasseto, Jo?o V.

, p. 2415 - 2417 (2007/10/03)

Alkylseleno and alkyltelluro groups are efficient non-transferable ligands of cyanocuprates in 1,4-addition reactions to enones.

METALLORGANISCHE VERBINDUNGEN DER LANTHANOIDE XXXV. BIS(TETRAMETHYLETHYLENDIAMIN)LITHIUM TETRAKIS-t-BUTYLLUTETAT(III):SYNTHESE, MOLEKUELSTRUKTUR UND REAKTIVES VERHALTEN GEGENUEBER α,β-UNGESAETTIGTEN CARBONYLVERBINDUNGEN

Schumann, Herbert,Genthe, Wolfgang,Hahn, Ekkehardt,Pickardt, Joachim,Schwarz, Helmut,Eckart, Klaus

, p. 215 - 226 (2007/10/02)

LuCl3 reacts with t-butyllithium in the presence of ether and tetramethylethylene diamine (tmed) to form , the structure of which has been elucidated through complete X-ray analysis.The crystals are orthorhombic with a 20.995(9), b 18.310(7), c 9.527(2) Angstroem, space group P21ab, Z = 4, D(calcd) 1.17 g cm-3, R = 0.035, and 2471 observed reflections.The compound undergoes 1,2-addition to cinnamic aldehyde, benzalacetone, 1-phenylbutene-2-methyl-3-one, 2-methylbutene-3-one and cyclohexanone, respectively, to give after hydrolysis of the reaction mixture α-t-butyl-substituted enoles.The reaction products were identified by means of GC/MS methods.

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