Cas 454251-82-2,(1R,3aR,3bS,4aR,6R,8aS,10aR)-3,6,9,9-Tetramethyl-1-phenyl-dodecahydro-4-oxa-3,9a-diaza-pentaleno[1,2-b]naphthalene

454251-82-2

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Basic information

Product Name: (1R,3aR,3bS,4aR,6R,8aS,10aR)-3,6,9,9-Tetramethyl-1-phenyl-dodecahydro-4-oxa-3,9a-diaza-pentaleno[1,2-b]naphthalene
Synonyms: (1R,3aR,3bS,4aR,6R,8aS,10aR)-3,6,9,9-Tetramethyl-1-phenyl-dodecahydro-4-oxa-3,9a-diaza-pentaleno[1,2-b]naphthalene
CAS NO:454251-82-2
Molecular Formula:
Molecular Weight: 354.536
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: (1R,3aR,3bS,4aR,6R,8aS,10aR)-3,6,9,9-Tetramethyl-1-phenyl-dodecahydro-4-oxa-3,9a-diaza-pentaleno[1,2-b]naphthalene(CAS DataBase Reference)
NIST Chemistry Reference: (1R,3aR,3bS,4aR,6R,8aS,10aR)-3,6,9,9-Tetramethyl-1-phenyl-dodecahydro-4-oxa-3,9a-diaza-pentaleno[1,2-b]naphthalene(454251-82-2)
EPA Substance Registry System: (1R,3aR,3bS,4aR,6R,8aS,10aR)-3,6,9,9-Tetramethyl-1-phenyl-dodecahydro-4-oxa-3,9a-diaza-pentaleno[1,2-b]naphthalene(454251-82-2)

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: 454251-82-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 454251-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,4,2,5 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 454251-82:
(8*4)+(7*5)+(6*4)+(5*2)+(4*5)+(3*1)+(2*8)+(1*2)=142
142 % 10 = 2
So 454251-82-2 is a valid CAS Registry Number.

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454251-82-2Relevant academic research and scientific papers

A novel synthesis of enantiopure octahydropyrrolo[3,4-b]pyrroles by intramolecular [3 + 2] dipolar cycloaddition on chiral perhydro-1,3-benzoxazines

Pedrosa, Rafael,Andres, Celia,De Las Heras, Laura,Nieto, Javier

, p. 2513 - 2516 (2007/10/03)

(Matrix presented) Condensation of N-substituted glycines with chiral 3-allyl-2-formyl perhydro-1,3-benzoxazines forms an azomethine ylide that cyclizes to give octahydropyrrolo[3,4-b]pyrrole derivatives. The [3 + 2] dipolar cycloadditions are stereoespec

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