Cas 1159174-77-2,(S)-1-(3-(4,4'-dimethoxytrityloxy)-2-hydroxypropyl)-N<sub>4</sub>-acetylcytosine

1159174-77-2

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Basic information

Product Name: (S)-1-(3-(4,4'-dimethoxytrityloxy)-2-hydroxypropyl)-N₄-acetylcytosine
Synonyms: (S)-1-(3-(4,4'-dimethoxytrityloxy)-2-hydroxypropyl)-N₄-acetylcytosine
CAS NO:1159174-77-2
Molecular Formula:
Molecular Weight: 529.593
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (S)-1-(3-(4,4'-dimethoxytrityloxy)-2-hydroxypropyl)-N₄-acetylcytosine(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-(3-(4,4'-dimethoxytrityloxy)-2-hydroxypropyl)-N₄-acetylcytosine(1159174-77-2)
EPA Substance Registry System: (S)-1-(3-(4,4'-dimethoxytrityloxy)-2-hydroxypropyl)-N₄-acetylcytosine(1159174-77-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1159174-77-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1159174-77-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,9,1,7 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1159174-77:
(9*1)+(8*1)+(7*5)+(6*9)+(5*1)+(4*7)+(3*4)+(2*7)+(1*7)=172
172 % 10 = 2
So 1159174-77-2 is a valid CAS Registry Number.

1159174-77-2Upstream product

1159174-77-2Downstream Products

1159174-80-7 C₃₉H₄₈N₅O₇P

1159174-77-2Relevant academic research and scientific papers

Improved phosphoramidite building blocks for the synthesis of the simplified nucleic acid GNA

Schlegel, Mark K.,Meggers, Eric

experimental part, p. 4615 - 4618 (2009/09/08)

(Chemical Equation Presented) An improved synthesis of glycol nucleic acids is reported using new phosphoramidite building blocks in which the exocyclic amino groups of adenine and guanine are protected as N-dimethylformamidines, whereas the amino group o

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