Cas 1374604-05-3,(5-methoxy-2-(2-(3-(2-propyl-1,3-dioxolan-2-yl)propyl)pyrrolidin-1-yl)phenyl)methanol

1374604-05-3

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Basic information

Product Name: (5-methoxy-2-(2-(3-(2-propyl-1,3-dioxolan-2-yl)propyl)pyrrolidin-1-yl)phenyl)methanol
Synonyms: (5-methoxy-2-(2-(3-(2-propyl-1,3-dioxolan-2-yl)propyl)pyrrolidin-1-yl)phenyl)methanol
CAS NO:1374604-05-3
Molecular Formula:
Molecular Weight: 363.497
EINECS: N/A
Product Categories: N/A
Mol File: 1374604-05-3.mol
Article Data: 1

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: (5-methoxy-2-(2-(3-(2-propyl-1,3-dioxolan-2-yl)propyl)pyrrolidin-1-yl)phenyl)methanol(CAS DataBase Reference)
NIST Chemistry Reference: (5-methoxy-2-(2-(3-(2-propyl-1,3-dioxolan-2-yl)propyl)pyrrolidin-1-yl)phenyl)methanol(1374604-05-3)
EPA Substance Registry System: (5-methoxy-2-(2-(3-(2-propyl-1,3-dioxolan-2-yl)propyl)pyrrolidin-1-yl)phenyl)methanol(1374604-05-3)

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: 1374604-05-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1374604-05-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,6,0 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1374604-05:
(9*1)+(8*3)+(7*7)+(6*4)+(5*6)+(4*0)+(3*4)+(2*0)+(1*5)=153
153 % 10 = 3
So 1374604-05-3 is a valid CAS Registry Number.

1374604-05-3Upstream product

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1374604-05-3Relevant articles and documents

Intramolecular redox-triggered C-H functionalization

Jurberg, Igor D.,Peng, Bo,Woestefeld, Eckhard,Wasserloos, Maximilian,Maulide, Nuno

, p. 1950 - 1953 (2012/04/04)

Sacrifice for the team: A one-pot method achieves remote functionalization at the α-position of an amine moiety through the sacrificial reduction of a neighboring group. The process takes advantage of an intramolecular redox reaction, thereby avoiding the need for any external oxidants. This method was applied to a concise five-step total synthesis of indolizidine 167B.

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