Cas 1036709-20-2,N-(3-methoxypropyl)-N-(tert-butoxycarbonyl)-α-methyl-phenylalanine ethyl ester

1036709-20-2

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Basic information

Product Name: N-(3-methoxypropyl)-N-(tert-butoxycarbonyl)-α-methyl-phenylalanine ethyl ester
Synonyms: N-(3-methoxypropyl)-N-(tert-butoxycarbonyl)-α-methyl-phenylalanine ethyl ester
CAS NO:1036709-20-2
Molecular Formula:
Molecular Weight: 379.497
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: N-(3-methoxypropyl)-N-(tert-butoxycarbonyl)-α-methyl-phenylalanine ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N-(3-methoxypropyl)-N-(tert-butoxycarbonyl)-α-methyl-phenylalanine ethyl ester(1036709-20-2)
EPA Substance Registry System: N-(3-methoxypropyl)-N-(tert-butoxycarbonyl)-α-methyl-phenylalanine ethyl ester(1036709-20-2)

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: 1036709-20-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1036709-20-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,7,0 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1036709-20:
(9*1)+(8*0)+(7*3)+(6*6)+(5*7)+(4*0)+(3*9)+(2*2)+(1*0)=132
132 % 10 = 2
So 1036709-20-2 is a valid CAS Registry Number.

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1036709-20-2Relevant academic research and scientific papers

Powdered KOH in OMSO: An efficient base for asymmetric cyclization via memory of chirality at ambient temperature

Kawabata, Takeo,Moriyama, Katsuhiko,Kawakami, Shimpei,Tsubaki, Kazunori

, p. 4153 - 4157 (2008)

Enolate chemistry has been extensively used for stereoselective C-C bond formation, in which metal amide bases are frequently employed in strictly anhydrous solvents at low temperatures. However, we found that asymmetric intramolecular C-C bond formation

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