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Benzoxazole, 2-(cyclohexylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104462-83-1

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104462-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104462-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,6 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104462-83:
(8*1)+(7*0)+(6*4)+(5*4)+(4*6)+(3*2)+(2*8)+(1*3)=101
101 % 10 = 1
So 104462-83-1 is a valid CAS Registry Number.

104462-83-1SDS

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-(cyclohexylmethyl)benzo[d]oxazole

1.2 Other means of identification

Product number -
Other names 2-cyclohexylmethyl-1,3-benzoxazole

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:104462-83-1 SDS

104462-83-1Downstream Products

104462-83-1Relevant academic research and scientific papers

Catalytic C-H Bond Alkylation of Azoles with Alkyl Halides Mediated by Nickel(II) Complexes of Phenanthridine-Based N^ N-^ N Pincer Ligands

Braun, Jason D.,Herbert, David E.,Mandapati, Pavan,Sidhu, Baldeep K.,Wilson, Gabrielle

, p. 1989 - 1997 (2020/06/08)

Ni(II) complexes supported by tridentate N^N-^N diarylamido pincer-type ligands have been demonstrated to act as active catalysts in the carbon-carbon bond forming alkylation of azoles using unactivated alkyl halides. Here, we show that benzann

The nickel/copper-catalyzed direct alkylation of heterocyclic C-H bonds

Vechorkin, Oleg,Proust, Valerie,Hu, Xile

supporting information; experimental part, p. 3061 - 3064 (2010/07/05)

(Figure Presented) Too selective: A general and straightforward protocol for the cross-coupling of non-activated alkyl halides with heterocyclic C-H bonds has been developed. The transformation is chemo- and regioselective and many functional groups on both coupling partners are tolerated. The method employs cheap nickel/copper catalysts, and expands significantly the scope of C-H functionalization (see scheme).

Microbial hydroxylation of 2-cycloalkylbenzoxazoles. Part II. Determination of product structures and enhancement of enantiomeric excess

De Raadt,Griengl,Petsch,Plachota,Schoo,Weber,Braunegg,Kopper,Kreiner,Zeiser

, p. 473 - 490 (2007/10/03)

The determinations of product structures obtained in the microbial hydroxylations of various 2-cycloalkyl-1,3-benzoxazoles using Cunninghamella blakesleeana DSM 1906 and Bacillus megaterium DSM 32 are described. The initially low e.e of 3-(benz-1,3-oxazol

The Condensation Product of 2-Aminophenol and Glyoxal. Structure and Photochemistry

Tauer, Erich,Grellmann, Karl-Heinz,Kaufmann, Eckhard,Noltemeyer, Mathias

, p. 3316 - 3325 (2007/10/02)

It has been shown by X-ray analysis that the condensation product of 2-aminophenol and glyoxal is 5a,6,11a,12-tetrahydrobenzoxazinobenzoxazine (5) and not, as generally assumed, 2,2'-bibenzoxazoline (4).The structure of 5 is preserved if

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