Cas 68506-19-4,Diphenylmethyl-2-(1R,5S)-3-phenyl-7-oxo-4-oxa-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl)-3,4-dichlor-3-methylbutanoat

68506-19-4

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Basic information

Product Name: Diphenylmethyl-2-(1R,5S)-3-phenyl-7-oxo-4-oxa-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl)-3,4-dichlor-3-methylbutanoat
Synonyms:
CAS NO:68506-19-4
Molecular Formula:
Molecular Weight: 523.416
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: Diphenylmethyl-2-(1R,5S)-3-phenyl-7-oxo-4-oxa-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl)-3,4-dichlor-3-methylbutanoat(CAS DataBase Reference)
NIST Chemistry Reference: Diphenylmethyl-2-(1R,5S)-3-phenyl-7-oxo-4-oxa-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl)-3,4-dichlor-3-methylbutanoat(68506-19-4)
EPA Substance Registry System: Diphenylmethyl-2-(1R,5S)-3-phenyl-7-oxo-4-oxa-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl)-3,4-dichlor-3-methylbutanoat(68506-19-4)

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: 68506-19-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 68506-19-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,5,0 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68506-19:
(7*6)+(6*8)+(5*5)+(4*0)+(3*6)+(2*1)+(1*9)=144
144 % 10 = 4
So 68506-19-4 is a valid CAS Registry Number.

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68506-19-4Relevant academic research and scientific papers

STEREOCONTROLLED, STRAIGHTFORWARD SYNTHESIS OF 3-SUBSTITUTED METHYL 7α-METHOXY-1-OXACEPHEMS

Yoshioka, Mitsuru,Tsui, Teruji,Uyeo, Shoichiro,Yamamoto, Sadao,Aoki, Tsutomu,at al.

, p. 351 - 354 (2007/10/02)

Stereocontrolled and industrially feasible synthesis of a new antibiotic 1a and related derivates, which is characterized by using all the carbon atoms of the penicillin skeleton, is described.

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