Cas 536730-56-0,5,8-Dioxa-2,11-diazadodecanedioic acid, 4,9-dioxo-3,10-bis(phenylmethyl)-, bis(1,1-dimethylethyl) ester, (3S,10S)-

536730-56-0

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Basic information

Product Name: 5,8-Dioxa-2,11-diazadodecanedioic acid, 4,9-dioxo-3,10-bis(phenylmethyl)-, bis(1,1-dimethylethyl) ester, (3S,10S)-
Synonyms:
CAS NO:536730-56-0
Molecular Formula: C30H40N2O8
Molecular Weight: 556.656
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: 5,8-Dioxa-2,11-diazadodecanedioic acid, 4,9-dioxo-3,10-bis(phenylmethyl)-, bis(1,1-dimethylethyl) ester, (3S,10S)-(CAS DataBase Reference)
NIST Chemistry Reference: 5,8-Dioxa-2,11-diazadodecanedioic acid, 4,9-dioxo-3,10-bis(phenylmethyl)-, bis(1,1-dimethylethyl) ester, (3S,10S)-(536730-56-0)
EPA Substance Registry System: 5,8-Dioxa-2,11-diazadodecanedioic acid, 4,9-dioxo-3,10-bis(phenylmethyl)-, bis(1,1-dimethylethyl) ester, (3S,10S)-(536730-56-0)

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: 536730-56-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 536730-56-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,6,7,3 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 536730-56:
(8*5)+(7*3)+(6*6)+(5*7)+(4*3)+(3*0)+(2*5)+(1*6)=160
160 % 10 = 0
So 536730-56-0 is a valid CAS Registry Number.

536730-56-0Upstream product

536730-56-0Downstream Products

536730-37-7 (2S)-2-(tert-butoxycarbonyl-methoxymethylamino)-3-phenylpropionic acid 2-[(2S)-2-(tert-butoxycarbonyl-methoxymethylamino)-3-phenylpropionyloxy]-ethyl ester

536730-56-0Relevant academic research and scientific papers

Control of the enantioselectivity of alkylation of phenylalanine derivatives by regulation of the aggregate structure of chiral enolate intermediates

Kawabata, Takeo,Kawakami, Shin-Pei,Shimada, Shoko,Fuji, Kaoru

, p. 965 - 974 (2003)

Two strategies were introduced for the control of enantioselectivity of alkylation of phenylalanine derivatives by regulation of the aggregate structure of chiral enolate intermediates. Use of amino acid-dimers, 6 and 15, was effective to minimize solvent

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