Cas 313342-74-4,(S)-1-((2R,4S,5R)-4-Hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-methyl-5-phenylacetyl-dihydro-pyrimidine-2,4-dione

313342-74-4

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Basic information

Product Name: (S)-1-((2R,4S,5R)-4-Hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-methyl-5-phenylacetyl-dihydro-pyrimidine-2,4-dione
Synonyms:
CAS NO:313342-74-4
Molecular Formula:
Molecular Weight: 362.382
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-((2R,4S,5R)-4-Hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-methyl-5-phenylacetyl-dihydro-pyrimidine-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-((2R,4S,5R)-4-Hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-methyl-5-phenylacetyl-dihydro-pyrimidine-2,4-dione(313342-74-4)
EPA Substance Registry System: (S)-1-((2R,4S,5R)-4-Hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-methyl-5-phenylacetyl-dihydro-pyrimidine-2,4-dione(313342-74-4)

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: 313342-74-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 313342-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,3,4 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 313342-74:
(8*3)+(7*1)+(6*3)+(5*3)+(4*4)+(3*2)+(2*7)+(1*4)=104
104 % 10 = 4
So 313342-74-4 is a valid CAS Registry Number.

313342-74-4Upstream product

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313342-74-4Relevant academic research and scientific papers

Synthesis and deprotection of oligonucleotides under aprotic conditions

Chen, Tongqian,Fu, Jiasheng,Greenberg, Marc M.

, p. 3691 - 3694 (2000)

(matrix presented) Oligonucleotides containing an alkali-labile nucleotide are synthesized and deprotected using a synthetic method that eliminates the use of Bronsted acid and base. The development of a new family of exocyclic amine-protecting groups is an integral component of this approach.

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