Cas 1101103-86-9,(R)-ethyl 2-(tert-butoxycarbonyl(methoxymethyl)amino)-3-phenylpropanoate

1101103-86-9

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Basic information

Product Name: (R)-ethyl 2-(tert-butoxycarbonyl(methoxymethyl)amino)-3-phenylpropanoate
Synonyms: (R)-ethyl 2-(tert-butoxycarbonyl(methoxymethyl)amino)-3-phenylpropanoate
CAS NO:1101103-86-9
Molecular Formula:
Molecular Weight: 337.416
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: (R)-ethyl 2-(tert-butoxycarbonyl(methoxymethyl)amino)-3-phenylpropanoate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-ethyl 2-(tert-butoxycarbonyl(methoxymethyl)amino)-3-phenylpropanoate(1101103-86-9)
EPA Substance Registry System: (R)-ethyl 2-(tert-butoxycarbonyl(methoxymethyl)amino)-3-phenylpropanoate(1101103-86-9)

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: 1101103-86-9(Hazardous Substances Data)

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1101103-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1101103-86-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,1,1,0 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1101103-86:
(9*1)+(8*1)+(7*0)+(6*1)+(5*1)+(4*0)+(3*3)+(2*8)+(1*6)=59
59 % 10 = 9
So 1101103-86-9 is a valid CAS Registry Number.

1101103-86-9Upstream product

67-56-1 methanol

1101103-86-9Downstream Products

176796-27-3 2-tert-butoxycarbonylamino-3-phenyl-propionic acid ethyl ester

1101103-86-9Relevant academic research and scientific papers

A facile method for the preparation of MOM-protected carbamates

Barnes, David M.,Barkalow, Jufang,Plata, Daniel J.

supporting information; experimental part, p. 273 - 275 (2009/08/08)

(Chemical Equation Presented) A novel method for the preparation of MOM-protected carbamates is described that avoids the use of MOM-Cl, a regulated carcinogen. The two-step, one-pot procedure generates a reactive N-chloromethyl carbamate that is quenched

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