Cas 69810-49-7,(R)-((S)-2-Oxo-3-phenylacetylamino-azetidin-1-yl)-phenyl-acetic acid methyl ester

69810-49-7

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Basic information

Product Name: (R)-((S)-2-Oxo-3-phenylacetylamino-azetidin-1-yl)-phenyl-acetic acid methyl ester
Synonyms: (R)-((S)-2-Oxo-3-phenylacetylamino-azetidin-1-yl)-phenyl-acetic acid methyl ester
CAS NO:69810-49-7
Molecular Formula:
Molecular Weight: 352.39
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: (R)-((S)-2-Oxo-3-phenylacetylamino-azetidin-1-yl)-phenyl-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-((S)-2-Oxo-3-phenylacetylamino-azetidin-1-yl)-phenyl-acetic acid methyl ester(69810-49-7)
EPA Substance Registry System: (R)-((S)-2-Oxo-3-phenylacetylamino-azetidin-1-yl)-phenyl-acetic acid methyl ester(69810-49-7)

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: 69810-49-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 69810-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,1 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69810-49:
(7*6)+(6*9)+(5*8)+(4*1)+(3*0)+(2*4)+(1*9)=157
157 % 10 = 7
So 69810-49-7 is a valid CAS Registry Number.

69810-49-7Upstream product

96738-19-1 (1R,3R,8aR)-2-Oxo-1-phenylacetylamino-1,8a-dihydro-2H,3H-8-thia-2a-aza-cyclobuta[b]naphthalene-3-carboxylic acid methyl ester

69810-49-7Downstream Products

69810-49-7Relevant academic research and scientific papers

Synthesis of Tricyclic Cephalosporins

Hatanaka, Minoru,Yamamoto, Yuichi,Ishimaru, Toshiyasu

, p. 1705 - 1706 (2007/10/02)

Cephalosporin 3'-triphenylphosphonium ylide (1) reacted with acrylaldehyde to give the C-3,C-4 tricyclic compound (3), while the sulphoxide of the ylide (1) upon similar treatment gave the C-2,C-3 tricyclic compound (4) which was converted into the ring-fused analogue (7) of nocardin; desulphurization of this compound afforded the nocardicin nucleus (10).

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