Cas 1334430-59-9,(S)-methyl 2-((3S,4S)-4-hydroxy-1,5-diphenylpent-1-yn-3-ylamino)-3-phenylpropanoate

1334430-59-9

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Basic information

Product Name: (S)-methyl 2-((3S,4S)-4-hydroxy-1,5-diphenylpent-1-yn-3-ylamino)-3-phenylpropanoate
Synonyms:
CAS NO:1334430-59-9
Molecular Formula:
Molecular Weight: 413.516
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)-methyl 2-((3S,4S)-4-hydroxy-1,5-diphenylpent-1-yn-3-ylamino)-3-phenylpropanoate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-methyl 2-((3S,4S)-4-hydroxy-1,5-diphenylpent-1-yn-3-ylamino)-3-phenylpropanoate(1334430-59-9)
EPA Substance Registry System: (S)-methyl 2-((3S,4S)-4-hydroxy-1,5-diphenylpent-1-yn-3-ylamino)-3-phenylpropanoate(1334430-59-9)

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: 1334430-59-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1334430-59-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,4,3 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1334430-59:
(9*1)+(8*3)+(7*3)+(6*4)+(5*4)+(4*3)+(3*0)+(2*5)+(1*9)=129
129 % 10 = 9
So 1334430-59-9 is a valid CAS Registry Number.

1334430-59-9Upstream product

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1334430-59-9Relevant academic research and scientific papers

Catalytic diastereoselective petasis reactions

Muncipinto, Giovanni,Moquist, Philip N.,Schreiber, Stuart L.,Schaus, Scott E.

supporting information; experimental part, p. 8172 - 8175 (2011/10/18)

Multicomponent Petasis reactions: The first diastereoselective Petasis reaction catalyzed by chiral biphenols that enables the synthesis of syn and anti β-amino alcohols in pure form has been developed. The reaction exploits a multicomponent approach that

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