Cas 1228565-11-4,(2Z,5E)-ethyl 3-amino-4-(tert-butyldimethylsilyl)oxy-2-ethyl-5-methyl-6-phenylhexa-2,5-dienoate

1228565-11-4

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Basic information

Product Name: (2Z,5E)-ethyl 3-amino-4-(tert-butyldimethylsilyl)oxy-2-ethyl-5-methyl-6-phenylhexa-2,5-dienoate
Synonyms: (2Z,5E)-ethyl 3-amino-4-(tert-butyldimethylsilyl)oxy-2-ethyl-5-methyl-6-phenylhexa-2,5-dienoate
CAS NO:1228565-11-4
Molecular Formula:
Molecular Weight: 403.637
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: (2Z,5E)-ethyl 3-amino-4-(tert-butyldimethylsilyl)oxy-2-ethyl-5-methyl-6-phenylhexa-2,5-dienoate(CAS DataBase Reference)
NIST Chemistry Reference: (2Z,5E)-ethyl 3-amino-4-(tert-butyldimethylsilyl)oxy-2-ethyl-5-methyl-6-phenylhexa-2,5-dienoate(1228565-11-4)
EPA Substance Registry System: (2Z,5E)-ethyl 3-amino-4-(tert-butyldimethylsilyl)oxy-2-ethyl-5-methyl-6-phenylhexa-2,5-dienoate(1228565-11-4)

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: 1228565-11-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1228565-11-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,5,6 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1228565-11:
(9*1)+(8*2)+(7*2)+(6*8)+(5*5)+(4*6)+(3*5)+(2*1)+(1*1)=154
154 % 10 = 4
So 1228565-11-4 is a valid CAS Registry Number.

1228565-11-4Upstream product

1228565-11-4Downstream Products

1228565-12-5 C₁₇H₂₃NO₃

1228565-11-4Relevant academic research and scientific papers

Organocatalytic asymmetric aza-Nazarov cyclization of an azirine

Shimada, Naoyuki,Ashburn, Bradley O.,Basak, Ashok K.,Bow, William F.,Vicic, David A.,Tius, Marcus A.

supporting information; experimental part, p. 3774 - 3775 (2010/08/07)

An unusual organocatalytic asymmetric cyclization of a ketoazirine that is accompanied by a kinetic resolution leads to 4-hydroxy-3-oxo-1,2,3,6- tetrahydropyridine-2-carboxylates in >99/1 er.

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