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(S)-6-chloro-1-(4-methoxybenzyl)-2-oxo-4-(trifluoromethyl)-1,2,3,4-tetrahydroquinazoline-4-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1414889-09-0

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1414889-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1414889-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,4,8,8 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1414889-09:
(9*1)+(8*4)+(7*1)+(6*4)+(5*8)+(4*8)+(3*9)+(2*0)+(1*9)=180
180 % 10 = 0
So 1414889-09-0 is a valid CAS Registry Number.

1414889-09-0Downstream Products

1414889-09-0Relevant articles and documents

Organocatalytic enantioselective Strecker reaction of cyclic trifluoromethyl-ketoimines

Xie, Hexin,Song, Aiguo,Song, Xixi,Zhang, Xinshuai,Wang, Wei

supporting information, p. 1409 - 1411 (2013/04/23)

A quinine thiourea promoted enantioselective Strecker reaction of cyclic ketoimines with TMSCN has been developed. The process affords new enantioenriched trifluoromethyl dihydroquinazolinones in high yields and with high enantioselectivities. Copyright

Highly enantioselective organocatalytic Strecker reaction of cyclic N-acyl trifluoromethylketimines: Synthesis of anti-HIV drug DPC 083

Zhang, Fa-Guang,Zhu, Xiao-Yan,Li, Shen,Nie, Jing,Ma, Jun-An

supporting information, p. 11552 - 11554,3 (2012/12/12)

A highly efficient, organocatalytic, enantioselective Strecker reaction of cyclic N-acyl ketimines was developed for the preparation of enantioenriched cyclic α-amino nitriles with a quaternary carbon stereocentre and anti-HIV drug DPC 083. This journal is

Highly enantioselective organocatalytic Strecker reaction of cyclic N-acyl trifluoromethylketimines: Synthesis of anti-HIV drug DPC 083

Zhang, Fa-Guang,Zhu, Xiao-Yan,Li, Shen,Nie, Jing,Ma, Jun-An

supporting information, p. 11552 - 11554 (2013/01/15)

A highly efficient, organocatalytic, enantioselective Strecker reaction of cyclic N-acyl ketimines was developed for the preparation of enantioenriched cyclic α-amino nitriles with a quaternary carbon stereocentre and anti-HIV drug DPC 083. The Royal Society of Chemistry 2012.

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