Cas 231609-73-7,(2S,3S)-2-Benzyloxyamino-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ<sup>6</sup>-thia-4-aza-tricyclo[5.2.1.0<sup>1,5</sup>]dec-4-yl)-3-naphthalen-1-yl-pent-4-en-1-one

231609-73-7

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Basic information

Product Name: (2S,3S)-2-Benzyloxyamino-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-naphthalen-1-yl-pent-4-en-1-one
Synonyms: (2S,3S)-2-Benzyloxyamino-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-naphthalen-1-yl-pent-4-en-1-one
CAS NO:231609-73-7
Molecular Formula:
Molecular Weight: 544.715
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: (2S,3S)-2-Benzyloxyamino-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-naphthalen-1-yl-pent-4-en-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-2-Benzyloxyamino-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-naphthalen-1-yl-pent-4-en-1-one(231609-73-7)
EPA Substance Registry System: (2S,3S)-2-Benzyloxyamino-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-naphthalen-1-yl-pent-4-en-1-one(231609-73-7)

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: 231609-73-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 231609-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,1,6,0 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 231609-73:
(8*2)+(7*3)+(6*1)+(5*6)+(4*0)+(3*9)+(2*7)+(1*3)=117
117 % 10 = 7
So 231609-73-7 is a valid CAS Registry Number.

231609-73-7Upstream product

98978-42-8 (E)-1-(3-bromoprop-1-en-1-yl)naphthalene

231609-73-7Downstream Products

231609-73-7Relevant academic research and scientific papers

Asymmetric synthesis of L-azetidine-2-carboxylic acid and 3-substituted congeners - Conformationally constrained analogs of phenylalanine, naphthylalanine, and leucine

Hanessian, Stephen,Bernstein, Naomy,Yang, Rui-Yang,Maguire, Robert

, p. 1437 - 1442 (1999)

Enantiopure L-azetidine-2-carboxylic acid, the (3R)-phenyl, (3R)- naphthyl and (3S)-isopropyl analogs were prepared based on a zinc-mediated asymmetric addition of allylic halides to the camphor sultam derivative of glyoxylic acid O-benzyl oxime.

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