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Benzene, 1-bromo-4-(1-diazoethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66751-80-2

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66751-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66751-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,7,5 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66751-80:
(7*6)+(6*6)+(5*7)+(4*5)+(3*1)+(2*8)+(1*0)=152
152 % 10 = 2
So 66751-80-2 is a valid CAS Registry Number.

66751-80-2Relevant academic research and scientific papers

alpha-aryl or alkyl substituted borane adduct, preparation method and applications thereof

-

Paragraph 0305-0308; 0310-0313; 0315, (2020/01/25)

The invention relates to an alpha-aryl or alkyl substituted borane adduct, a preparation method and applications thereof, specifically to preparation of an alpha-aryl or alkyl substituted borane adduct by carrying out a reaction on hydrazone as an unstabl

Enantioselective Synthesis of Trisubstituted Allenes via Cu(I)-Catalyzed Coupling of Diazoalkanes with Terminal Alkynes

Chu, Wen-Dao,Zhang, Lei,Zhang, Zhikun,Zhou, Qi,Mo, Fanyang,Zhang, Yan,Wang, Jianbo

supporting information, p. 14558 - 14561 (2016/11/18)

A highly enantioselective synthesis of trisubstituted allenes has been achieved through Cu(I)-catalyzed cross-coupling of aryldiazoalkanes and terminal alkynes with chiral bisoxazoline ligands. Alkynyl migratory insertion of Cu(I) carbene is proposed as t

Catalytic Asymmetric Formal Insertion of Aryldiazoalkanes into the C-H Bond of Aldehydes: Synthesis of Enantioenriched Acyclic α-Tertiary Aryl Ketones

Kang, Byung Chul,Nam, Dong Guk,Hwang, Geum-Sook,Ryu, Do Hyun

supporting information, p. 4810 - 4813 (2015/10/12)

A novel, catalytic enantioselective route to synthesize a variety of α-tertiary aryl ketones via a boron Lewis acid promoted formal insertion of aryldiazoalkane into the C-H bond of both aromatic and aliphatic aldehydes is described. In the presence of ch

A significant barrier to 1,2 hydrogen migration in singlet 1-phenylethylidene. A laser flash photolysis study

Sugiyama, Michelle H.,Celebi, Sol,Platz, Matthew S.

, p. 966 - 973 (2007/10/02)

Laser flash photolysis of 1-phenyldiazoethane in heptane releases 1-phenylethylidene which can be intercepted with pyridine to form an ylide (λmax> = 475 nm). Oxygen trapping experiments indicate that relaxation of singlet 1-phenylethylidene to

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