Cas 1443232-25-4,(3aR,5R,6aR)-methyl 2-benzyl-5-(tert-butoxycarbonylamino)octahydrocyclopenta[c]pyrrole-3a-carboxylate fumarate

1443232-25-4

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Basic information

Product Name: (3aR,5R,6aR)-methyl 2-benzyl-5-(tert-butoxycarbonylamino)octahydrocyclopenta[c]pyrrole-3a-carboxylate fumarate
Synonyms: (3aR,5R,6aR)-methyl 2-benzyl-5-(tert-butoxycarbonylamino)octahydrocyclopenta[c]pyrrole-3a-carboxylate fumarate
CAS NO:1443232-25-4
Molecular Formula:
Molecular Weight: 490.554
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: (3aR,5R,6aR)-methyl 2-benzyl-5-(tert-butoxycarbonylamino)octahydrocyclopenta[c]pyrrole-3a-carboxylate fumarate(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,5R,6aR)-methyl 2-benzyl-5-(tert-butoxycarbonylamino)octahydrocyclopenta[c]pyrrole-3a-carboxylate fumarate(1443232-25-4)
EPA Substance Registry System: (3aR,5R,6aR)-methyl 2-benzyl-5-(tert-butoxycarbonylamino)octahydrocyclopenta[c]pyrrole-3a-carboxylate fumarate(1443232-25-4)

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: 1443232-25-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1443232-25-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,3,2,3 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1443232-25:
(9*1)+(8*4)+(7*4)+(6*3)+(5*2)+(4*3)+(3*2)+(2*2)+(1*5)=124
124 % 10 = 4
So 1443232-25-4 is a valid CAS Registry Number.

1443232-25-4Upstream product

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1443232-25-4Relevant academic research and scientific papers

Chiral aminocyclopentene-based cycloaddition strategies to bicyclic [3.3.0] rings

Cai, Chaozhong,Kang, Fu-An,Beauchamp, Derek A.,Sui, Zhihua,Russell, Ronald K.,Teleha, Christopher A.

, p. 651 - 656 (2013)

Two cycloaddition methods were applied to chiral protected aminocyclopentenes 2 and 9 and provided novel bicyclic products 3 and 4 in good yields. The explanation for the observed stereochemistry was based on the sterically encumbered β-face forcing the c

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