Cas 848983-65-3,2-Oxa-4,9,14-triazapentadeca-6,11-dien-15-oic acid, 5,13-bis(1-methylethyl)-3-oxo-1-phenyl-9-(phenylmethyl)-, phenylmethyl ester, (5S,6E,11E,13S)-

848983-65-3

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Basic information

Product Name: 2-Oxa-4,9,14-triazapentadeca-6,11-dien-15-oic acid, 5,13-bis(1-methylethyl)-3-oxo-1-phenyl-9-(phenylmethyl)-, phenylmethyl ester, (5S,6E,11E,13S)-
Synonyms:
CAS NO:848983-65-3
Molecular Formula: C37H47N3O4
Molecular Weight: 597.798
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: 2-Oxa-4,9,14-triazapentadeca-6,11-dien-15-oic acid, 5,13-bis(1-methylethyl)-3-oxo-1-phenyl-9-(phenylmethyl)-, phenylmethyl ester, (5S,6E,11E,13S)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Oxa-4,9,14-triazapentadeca-6,11-dien-15-oic acid, 5,13-bis(1-methylethyl)-3-oxo-1-phenyl-9-(phenylmethyl)-, phenylmethyl ester, (5S,6E,11E,13S)-(848983-65-3)
EPA Substance Registry System: 2-Oxa-4,9,14-triazapentadeca-6,11-dien-15-oic acid, 5,13-bis(1-methylethyl)-3-oxo-1-phenyl-9-(phenylmethyl)-, phenylmethyl ester, (5S,6E,11E,13S)-(848983-65-3)

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: 848983-65-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 848983-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,9,8 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 848983-65:
(8*8)+(7*4)+(6*8)+(5*9)+(4*8)+(3*3)+(2*6)+(1*5)=243
243 % 10 = 3
So 848983-65-3 is a valid CAS Registry Number.

848983-65-3Upstream product

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848983-65-3Relevant academic research and scientific papers

Convenient preparation of optically active N,N-bis(4-substituted-4- aminobutyl)amines

Tsubaki, Kazunori,Kusumoto, Tomokazu,Hayashi, Noriyuki,Tanima, Daisuke,Fuji, Kaoru,Kawabata, Takeo

, p. 739 - 743 (2007/10/03)

An efficient and convenient method for the synthesis of chiral triamines with two substituents at the α position to the terminal amino group (spermidine analogues) is described. These chiral N,N-bis(4-substituted-4- aminobutyl)amines may have anticancer a

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