Cas 357277-83-9,Glycine, N-[2-[1-[(5-hydroxypentyl)(phenylmethyl)amino]heptyl]-4-(phenylmethyl)- 5-oxazolyl]-N-methyl-, methyl ester

357277-83-9

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Basic information

Product Name: Glycine, N-[2-[1-[(5-hydroxypentyl)(phenylmethyl)amino]heptyl]-4-(phenylmethyl)- 5-oxazolyl]-N-methyl-, methyl ester
Synonyms:
CAS NO:357277-83-9
Molecular Formula: C33H47N3O4
Molecular Weight: 549.754
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: Glycine, N-[2-[1-[(5-hydroxypentyl)(phenylmethyl)amino]heptyl]-4-(phenylmethyl)- 5-oxazolyl]-N-methyl-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Glycine, N-[2-[1-[(5-hydroxypentyl)(phenylmethyl)amino]heptyl]-4-(phenylmethyl)- 5-oxazolyl]-N-methyl-, methyl ester(357277-83-9)
EPA Substance Registry System: Glycine, N-[2-[1-[(5-hydroxypentyl)(phenylmethyl)amino]heptyl]-4-(phenylmethyl)- 5-oxazolyl]-N-methyl-, methyl ester(357277-83-9)

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: 357277-83-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 357277-83-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,2,7 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 357277-83:
(8*3)+(7*5)+(6*7)+(5*2)+(4*7)+(3*7)+(2*8)+(1*3)=179
179 % 10 = 9
So 357277-83-9 is a valid CAS Registry Number.

357277-83-9Upstream product

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357277-83-9Relevant academic research and scientific papers

5-Aminooxazole as an internal traceless activator of C-terminal carboxylic acid: Rapid access to diversely functionalized cyclodepsipeptides

Bughin, Carine,Zhao, Gang,Bienayme, Hugues,Zhu, Jieping

, p. 1174 - 1184 (2007/10/03)

A conceptually novel macrolactonization protocol has been developed. It is a domino process involving a sequence of: 1) protonation of 5-aminooxazole leading to the electrophilic iminium salt; 2) trapping of the iminium species by the neighboring C-termin

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