Cas 1620204-76-3,(S)-methyl 3-(4-acetoxy-3-(phthalimidyl)phenyl)-2-(tert-butoxycarbonylamino)propanoate

1620204-76-3

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Basic information

Product Name: (S)-methyl 3-(4-acetoxy-3-(phthalimidyl)phenyl)-2-(tert-butoxycarbonylamino)propanoate
Synonyms:
CAS NO:1620204-76-3
Molecular Formula:
Molecular Weight: 482.49
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)-methyl 3-(4-acetoxy-3-(phthalimidyl)phenyl)-2-(tert-butoxycarbonylamino)propanoate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-methyl 3-(4-acetoxy-3-(phthalimidyl)phenyl)-2-(tert-butoxycarbonylamino)propanoate(1620204-76-3)
EPA Substance Registry System: (S)-methyl 3-(4-acetoxy-3-(phthalimidyl)phenyl)-2-(tert-butoxycarbonylamino)propanoate(1620204-76-3)

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: 1620204-76-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1620204-76-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,2,0 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1620204-76:
(9*1)+(8*6)+(7*2)+(6*0)+(5*2)+(4*0)+(3*4)+(2*7)+(1*6)=113
113 % 10 = 3
So 1620204-76-3 is a valid CAS Registry Number.

1620204-76-3Upstream product

3481-09-2 N-chlorophthalimide

1620204-76-3Downstream Products

1620204-76-3Relevant academic research and scientific papers

Nitrogen-centered radical-mediated C-H imidation of arenes and heteroarenes via visible light induced photocatalysis

Kim, Hyejin,Kim, Taehoon,Lee, Dong Gil,Roh, Sang Weon,Lee, Chulbom

supporting information, p. 9273 - 9276 (2014/08/05)

The C-H imidation of arenes and heteroarenes has been achieved via visible light induced photocatalysis. In the presence of an iridium(iii) photoredox catalyst, the reaction of aromatic substrates with N-chlorophthalimide furnishes the N-aryl products at room temperature through a nitrogen-centered radical mediated aromatic substitution.

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