Cas 206987-55-5,[(S)-2-(4-Ethoxy-phenyl)-1-formyl-ethyl]-carbamic acid benzyl ester

206987-55-5

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Basic information

Product Name: [(S)-2-(4-Ethoxy-phenyl)-1-formyl-ethyl]-carbamic acid benzyl ester
Synonyms: [(S)-2-(4-Ethoxy-phenyl)-1-formyl-ethyl]-carbamic acid benzyl ester
CAS NO:206987-55-5
Molecular Formula:
Molecular Weight: 327.38
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: [(S)-2-(4-Ethoxy-phenyl)-1-formyl-ethyl]-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-2-(4-Ethoxy-phenyl)-1-formyl-ethyl]-carbamic acid benzyl ester(206987-55-5)
EPA Substance Registry System: [(S)-2-(4-Ethoxy-phenyl)-1-formyl-ethyl]-carbamic acid benzyl ester(206987-55-5)

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: 206987-55-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 206987-55-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,9,8 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 206987-55:
(8*2)+(7*0)+(6*6)+(5*9)+(4*8)+(3*7)+(2*5)+(1*5)=165
165 % 10 = 5
So 206987-55-5 is a valid CAS Registry Number.

206987-55-5Upstream product

158043-52-8 N-benzyloxycarbonyl-[S-1-(4-ethoxybenzyl)-2-hydroxyethyl]carboxamide

206987-55-5Downstream Products

206987-55-5Relevant academic research and scientific papers

Efficient synthesis of the gadolinium complex of a new C2-symmetric tetramine

Harre, Michael,Nickisch, Klaus,Schulz, Claudia,Weinmann, Hilmar

, p. 2555 - 2558 (1998)

A short and efficient synthesis of the substituted tetramines 2a and 7 and of the gadolinium complex 1 was developed starting from the Cbz-protected amino alcohol 3. Key steps of the synthesis are the optimized bleach oxidation of enantiopure alcohols and

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