Cas 737805-71-9,Acetic acid (2S,3S,4S)-4-iodo-2-(4-methoxy-benzyl)-1-(9-phenyl-9H-fluoren-9-yl)-pyrrolidin-3-yl ester

737805-71-9

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Basic information

Product Name: Acetic acid (2S,3S,4S)-4-iodo-2-(4-methoxy-benzyl)-1-(9-phenyl-9H-fluoren-9-yl)-pyrrolidin-3-yl ester
Synonyms: Acetic acid (2S,3S,4S)-4-iodo-2-(4-methoxy-benzyl)-1-(9-phenyl-9H-fluoren-9-yl)-pyrrolidin-3-yl ester
CAS NO:737805-71-9
Molecular Formula:
Molecular Weight: 615.511
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: Acetic acid (2S,3S,4S)-4-iodo-2-(4-methoxy-benzyl)-1-(9-phenyl-9H-fluoren-9-yl)-pyrrolidin-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2S,3S,4S)-4-iodo-2-(4-methoxy-benzyl)-1-(9-phenyl-9H-fluoren-9-yl)-pyrrolidin-3-yl ester(737805-71-9)
EPA Substance Registry System: Acetic acid (2S,3S,4S)-4-iodo-2-(4-methoxy-benzyl)-1-(9-phenyl-9H-fluoren-9-yl)-pyrrolidin-3-yl ester(737805-71-9)

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: 737805-71-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 737805-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,7,8,0 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 737805-71:
(8*7)+(7*3)+(6*7)+(5*8)+(4*0)+(3*5)+(2*7)+(1*1)=189
189 % 10 = 9
So 737805-71-9 is a valid CAS Registry Number.

737805-71-9Upstream product

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737805-71-9Relevant academic research and scientific papers

Stereodivergent and regioselective synthesis of 3,4-cis- and 3,4-trans-pyrrolidinediols from α-amino acids

Kim, Jin Hyo,Long, Marcus J. C.,Kim, Jun Young,Park, Ki Hun

, p. 2273 - 2276 (2007/10/03)

Highly stereodivergent Woodward-Prevost reaction applied to iodoacetates derived from homochiral α-amino acids afforded enantiopure 3,4-cis- and 3,4-trans-pyrrolidinediol derivatives, with control over the protecting group, allowing for differential prote

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