Cas 1217897-85-2,S-ethyl 2-cyano-2-N<sub>.</sub>N'-di(tert-butoxycarbonyl)hydrazino-3-(4-methoxyphenyl)propanethioate

1217897-85-2

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Basic information

Product Name: S-ethyl 2-cyano-2-N_.N'-di(tert-butoxycarbonyl)hydrazino-3-(4-methoxyphenyl)propanethioate
Synonyms: S-ethyl 2-cyano-2-N_.N'-di(tert-butoxycarbonyl)hydrazino-3-(4-methoxyphenyl)propanethioate
CAS NO:1217897-85-2
Molecular Formula:
Molecular Weight: 479.598
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-ethyl 2-cyano-2-N_.N'-di(tert-butoxycarbonyl)hydrazino-3-(4-methoxyphenyl)propanethioate(CAS DataBase Reference)
NIST Chemistry Reference: S-ethyl 2-cyano-2-N_.N'-di(tert-butoxycarbonyl)hydrazino-3-(4-methoxyphenyl)propanethioate(1217897-85-2)
EPA Substance Registry System: S-ethyl 2-cyano-2-N_.N'-di(tert-butoxycarbonyl)hydrazino-3-(4-methoxyphenyl)propanethioate(1217897-85-2)

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: 1217897-85-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1217897-85-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,8,9 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1217897-85:
(9*1)+(8*2)+(7*1)+(6*7)+(5*8)+(4*9)+(3*7)+(2*8)+(1*5)=192
192 % 10 = 2
So 1217897-85-2 is a valid CAS Registry Number.

1217897-85-2Upstream product

1217897-85-2Downstream Products

1217897-85-2Relevant academic research and scientific papers

Enantioselective electrophilic amination of α-cyanothioacetates with azodicarboxylates catalyzed by an axially chiral guanidine base

Terada, Masahiro,Tsushima, Daisuke,Nakano, Megumi

, p. 2817 - 2821 (2009)

An enantioselective electrophilic amination of α-substituted cyanothioacetates with azodicarboxylate is demonstrated using an axially chiral guanidine as a chiral Bronsted base catalyst. The corresponding product, having a quaternary stereogenie center at

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