Cas 1421074-35-2,ethyl (2S,3R,4S)-4-((tert-butoxycarbonyl)amino)-3-formyl-2-((4-methoxyphenyl)amino)-4-(o-tolyl)butanoate

1421074-35-2

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Basic information

Product Name: ethyl (2S,3R,4S)-4-((tert-butoxycarbonyl)amino)-3-formyl-2-((4-methoxyphenyl)amino)-4-(o-tolyl)butanoate
Synonyms:
CAS NO:1421074-35-2
Molecular Formula:
Molecular Weight: 470.566
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: ethyl (2S,3R,4S)-4-((tert-butoxycarbonyl)amino)-3-formyl-2-((4-methoxyphenyl)amino)-4-(o-tolyl)butanoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl (2S,3R,4S)-4-((tert-butoxycarbonyl)amino)-3-formyl-2-((4-methoxyphenyl)amino)-4-(o-tolyl)butanoate(1421074-35-2)
EPA Substance Registry System: ethyl (2S,3R,4S)-4-((tert-butoxycarbonyl)amino)-3-formyl-2-((4-methoxyphenyl)amino)-4-(o-tolyl)butanoate(1421074-35-2)

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: 1421074-35-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1421074-35-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,1,0,7 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1421074-35:
(9*1)+(8*4)+(7*2)+(6*1)+(5*0)+(4*7)+(3*4)+(2*3)+(1*5)=112
112 % 10 = 2
So 1421074-35-2 is a valid CAS Registry Number.

1421074-35-2Upstream product

124156-21-4 ethyl (4-methoxyphenylimino)acetate

1421074-35-2Downstream Products

1421074-35-2Relevant academic research and scientific papers

One-pot cross double-Mannich reaction of acetaldehyde catalyzed by a binaphthyl-based amino sulfonamide

Kano, Taichi,Sakamoto, Ryu,Yamaguchi, Yukako,Itoh, Ken-Ichi,Maruoka, Keiji

, p. 1118 - 1120 (2013)

A one-pot cross double-Mannich reaction of acetaldehyde was developed, and densely functionalized 1,3-diamines were obtained as a single stereoisomer by use of axially chiral amino sulfonamide (S)-1 as catalyst. Using this catalyst, the one-pot Mannich reaction-aminoxylation was also realized.

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