Cas 494838-52-7,2H-1,3-Diazepin-2-one, 1,3,4,7-tetrahydro-4,7-bis(2-methylpropyl)-1,3-bis(phenylmethyl)-, (4S,7S)-

494838-52-7

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Basic information

Product Name: 2H-1,3-Diazepin-2-one, 1,3,4,7-tetrahydro-4,7-bis(2-methylpropyl)-1,3-bis(phenylmethyl)-, (4S,7S)-
Synonyms:
CAS NO:494838-52-7
Molecular Formula: C27H36N2O
Molecular Weight: 404.596
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: 2H-1,3-Diazepin-2-one, 1,3,4,7-tetrahydro-4,7-bis(2-methylpropyl)-1,3-bis(phenylmethyl)-, (4S,7S)-(CAS DataBase Reference)
NIST Chemistry Reference: 2H-1,3-Diazepin-2-one, 1,3,4,7-tetrahydro-4,7-bis(2-methylpropyl)-1,3-bis(phenylmethyl)-, (4S,7S)-(494838-52-7)
EPA Substance Registry System: 2H-1,3-Diazepin-2-one, 1,3,4,7-tetrahydro-4,7-bis(2-methylpropyl)-1,3-bis(phenylmethyl)-, (4S,7S)-(494838-52-7)

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: 494838-52-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 494838-52-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,4,8,3 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 494838-52:
(8*4)+(7*9)+(6*4)+(5*8)+(4*3)+(3*8)+(2*5)+(1*2)=207
207 % 10 = 7
So 494838-52-7 is a valid CAS Registry Number.

494838-52-7Upstream product

494838-52-7Downstream Products

167826-76-8 (4S,5R,6S,7S)-1,3-Dibenzyl-5,6-dihydroxy-4,7-diisobutyl-[1,3]diazepan-2-one

494838-52-7Relevant academic research and scientific papers

A Concise Route to Structurally Diverse DMP 323 Analogues via Highly Functionalized 1,4-Diamines

McReynolds, Matthew D.,Sprott, Kevin T.,Hanson, Paul R.

, p. 4673 - 4676 (2007/10/03)

(Matrix Presented) The utility of functionalized 1,4-diamines, produced via a temporary phosphorus tether (P-tether)/ring-closing metathesis (RCM)/hydrolysis sequence, is demonstrated in the synthesis of structurally diverse DMP 323 analogues. These 1,4-d

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