Cas 1035913-54-2,[(S)-1-(2-(benzylsulfanyl)pyrimidin-4-yl)pyrrolidin-2-yl]methanol

1035913-54-2

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Basic information

Product Name: [(S)-1-(2-(benzylsulfanyl)pyrimidin-4-yl)pyrrolidin-2-yl]methanol
Synonyms: [(S)-1-(2-(benzylsulfanyl)pyrimidin-4-yl)pyrrolidin-2-yl]methanol
CAS NO:1035913-54-2
Molecular Formula:
Molecular Weight: 301.412
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-(2-(benzylsulfanyl)pyrimidin-4-yl)pyrrolidin-2-yl]methanol(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-1-(2-(benzylsulfanyl)pyrimidin-4-yl)pyrrolidin-2-yl]methanol(1035913-54-2)
EPA Substance Registry System: [(S)-1-(2-(benzylsulfanyl)pyrimidin-4-yl)pyrrolidin-2-yl]methanol(1035913-54-2)

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: 1035913-54-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1035913-54-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,5,9,1 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1035913-54:
(9*1)+(8*0)+(7*3)+(6*5)+(5*9)+(4*1)+(3*3)+(2*5)+(1*4)=132
132 % 10 = 2
So 1035913-54-2 is a valid CAS Registry Number.

1035913-54-2Upstream product

1035913-22-4 tert-butyl (S)-2-((2-(benzylsulfanyl)pyrimidin-4-yloxy)-methyl)pyrrolidine-1-carboxylate

1035913-54-2Downstream Products

1035913-54-2Relevant academic research and scientific papers

Synthesis of pyrimidinyl arylglycines through subsequent Mitsunobu and Petasis reactions

Font, David,Heras, Montserrat,Villalgordo, José M.

, p. 5226 - 5235 (2008/09/21)

The synthesis of highly functionalized pyrimidinyl arylglycines is presented. The highlight in our synthetic sequence includes selective O-alkylation of 2-(benzylsulfanyl)-4(3H)-pyrimidinones with N-Boc β-aminoalcohols under Mitsunobu conditions, Petasis

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