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1-(2-nitrophenyl)propane-1,3-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

168329-41-7

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168329-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 168329-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,3,2 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 168329-41:
(8*1)+(7*6)+(6*8)+(5*3)+(4*2)+(3*9)+(2*4)+(1*1)=157
157 % 10 = 7
So 168329-41-7 is a valid CAS Registry Number.

168329-41-7Relevant academic research and scientific papers

Genosnip: SNP genotyping by MALDI-TOF MS using photocleavable oligonucleotides

Wenzel,Elssner,Fahr,Bimmler,Richter,Thomas,Kostrzewa

, p. 1579 - 1581 (2003)

A photocleavable o-nitrobenzyl CE phosphoramidite building-block was synthesised and incorporated within oligonucleotides. After allele-specific primer extension, desalting was performed using genostrep purification plates. Release of the SNP information

Photocleavable morpholino oligos with integral photolinkers for modulating the activity of any selected gene transcript by exposure to light

-

Paragraph 0075; 0076, (2013/03/26)

Morpholinos are widely used to block the activity of selected single-stranded genetic sequences. This invention comprises Morpholinos containing one or more integral photolinkers (Photo-Morpholinos) wherein the photolinkers are directly incorporated into

Tandem catalysis by lipase in a vinyl acetate-mediated cross-aldol reaction

Kumar, Manjeet,Shah, Bhahwal A.,Taneja, Subhash C.

experimental part, p. 1207 - 1212 (2011/06/25)

The lipase Novozym435 (0.6% w/w) was used in tandem with organocatalysts in a first vinyl/isopropenyl acetate-mediated aldol reaction. The reaction was facilitated through the lipase-catalyzed in situ generation of acetaldehyde/acetone. The important features of the present methodology include the mild and facile reaction conditions, regenerability of the lipase, comparatively high yields and minimal side product formation.

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