Cas 1185735-33-4,[5-((1'S,2'R,4'S,5'S)-2'-hydroxymethyl-1'-azabicyclo[2.2.2]oct-5'-yl)-3-methyl-4-prop-1-ynyl-biphenyl-2-yl]methylketone

1185735-33-4

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Basic information

Product Name: [5-((1'S,2'R,4'S,5'S)-2'-hydroxymethyl-1'-azabicyclo[2.2.2]oct-5'-yl)-3-methyl-4-prop-1-ynyl-biphenyl-2-yl]methylketone
Synonyms:
CAS NO:1185735-33-4
Molecular Formula:
Molecular Weight: 387.522
EINECS: N/A
Product Categories: N/A
Mol File: 1185735-33-4.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-((1'S,2'R,4'S,5'S)-2'-hydroxymethyl-1'-azabicyclo[2.2.2]oct-5'-yl)-3-methyl-4-prop-1-ynyl-biphenyl-2-yl]methylketone(CAS DataBase Reference)
NIST Chemistry Reference: [5-((1'S,2'R,4'S,5'S)-2'-hydroxymethyl-1'-azabicyclo[2.2.2]oct-5'-yl)-3-methyl-4-prop-1-ynyl-biphenyl-2-yl]methylketone(1185735-33-4)
EPA Substance Registry System: [5-((1'S,2'R,4'S,5'S)-2'-hydroxymethyl-1'-azabicyclo[2.2.2]oct-5'-yl)-3-methyl-4-prop-1-ynyl-biphenyl-2-yl]methylketone(1185735-33-4)

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: 1185735-33-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1185735-33-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,5,7,3 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1185735-33:
(9*1)+(8*1)+(7*8)+(6*5)+(5*7)+(4*3)+(3*5)+(2*3)+(1*3)=174
174 % 10 = 4
So 1185735-33-4 is a valid CAS Registry Number.

1185735-33-4Upstream product

2809-69-0 2,4-hexadiyne

1185735-33-4Downstream Products

1185735-33-4Relevant articles and documents

Synthesis of new quinuclidine derivatives via Pd-mediated cross-coupling and cross-benzannulation reactions

T?t?s, Stefania,Fild, Manfred,Th?ne, Carsten,Grosu, Ion

, p. 6226 - 6235 (2009)

New functionalized quinuclidines were prepared via palladium-catalyzed addition reactions of terminal alkynes (donors) to internal alkynes (acceptors). The enantiopure terminal alkynes were derivatives of quincoridine and quincorine, two semi-natural Cinc

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