Cas 878157-34-7,Carbamic acid, [(2S)-3-(methoxymethylamino)-2-[[(4-methoxyphenyl)methyl]thio]-2-meth yl-3-oxopropyl]-, methyl ester

878157-34-7

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Basic information

Product Name: Carbamic acid, [(2S)-3-(methoxymethylamino)-2-[[(4-methoxyphenyl)methyl]thio]-2-meth yl-3-oxopropyl]-, methyl ester
Synonyms:
CAS NO:878157-34-7
Molecular Formula: C16H24N2O5S
Molecular Weight: 356.443
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: Carbamic acid, [(2S)-3-(methoxymethylamino)-2-[[(4-methoxyphenyl)methyl]thio]-2-meth yl-3-oxopropyl]-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [(2S)-3-(methoxymethylamino)-2-[[(4-methoxyphenyl)methyl]thio]-2-meth yl-3-oxopropyl]-, methyl ester(878157-34-7)
EPA Substance Registry System: Carbamic acid, [(2S)-3-(methoxymethylamino)-2-[[(4-methoxyphenyl)methyl]thio]-2-meth yl-3-oxopropyl]-, methyl ester(878157-34-7)

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: 878157-34-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 878157-34-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,1,5 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 878157-34:
(8*8)+(7*7)+(6*8)+(5*1)+(4*5)+(3*7)+(2*3)+(1*4)=217
217 % 10 = 7
So 878157-34-7 is a valid CAS Registry Number.

878157-34-7Upstream product

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878157-34-7Relevant academic research and scientific papers

SN2 reaction of sulfur nucleophiles with hindered sulfamidates: Enantioselective synthesis of α-methylisocysteine

Avenoza, Alberto,Busto, Jesus H.,Jimenez-Oses, Gonzalo,Peregrina, Jesus M.

, p. 1692 - 1695 (2006)

The work described here demonstrates that the five-membered cyclic α-methylisoserine-derived sulfamidate, (R)-1, behaves as an excellent chiral building block for the ring-opening reaction by S2 attack with sulfur nucleophiles at the quaternary carbon. As

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