Cas 119154-99-3,4-nitrobenzyl 8-benzamido-2-hydroxyl-5,9-dioxo-1,6-diazabicyclo<4.3.0>nonane-2-carboxylate

119154-99-3

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Basic information

Product Name: 4-nitrobenzyl 8-benzamido-2-hydroxyl-5,9-dioxo-1,6-diazabicyclo<4.3.0>nonane-2-carboxylate
Synonyms: 4-nitrobenzyl 8-benzamido-2-hydroxyl-5,9-dioxo-1,6-diazabicyclo<4.3.0>nonane-2-carboxylate
CAS NO:119154-99-3
Molecular Formula:
Molecular Weight: 468.423
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: 4-nitrobenzyl 8-benzamido-2-hydroxyl-5,9-dioxo-1,6-diazabicyclo<4.3.0>nonane-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: 4-nitrobenzyl 8-benzamido-2-hydroxyl-5,9-dioxo-1,6-diazabicyclo<4.3.0>nonane-2-carboxylate(119154-99-3)
EPA Substance Registry System: 4-nitrobenzyl 8-benzamido-2-hydroxyl-5,9-dioxo-1,6-diazabicyclo<4.3.0>nonane-2-carboxylate(119154-99-3)

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: 119154-99-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 119154-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,1,5 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 119154-99:
(8*1)+(7*1)+(6*9)+(5*1)+(4*5)+(3*4)+(2*9)+(1*9)=133
133 % 10 = 3
So 119154-99-3 is a valid CAS Registry Number.

119154-99-3Upstream product

119154-99-3Downstream Products

119155-00-9 sodium 8-benzamido-2-hydroxyl-5,9-dioxo-1,6-diazabicyclo<4.3.0>nonane-2-carboxylate

119154-99-3Relevant academic research and scientific papers

SYNTHESIS OF LACTIVICIN ANALOGUES

Tamura, Norikazu,Matsushita, Yoshihiro,Yoshioka, Kouichi,Ochiai, Michihiko

, p. 3231 - 3240 (1988)

Aza analogues of lactivicin (1), a recently discovered novel antibiotic, were prepared by an application of our earlier convenient synthesis of 1 and its derivatives.A 1-unsubstituted pyrazolidinone derivative bearing 2-aminothiazol-4-yl-(Z)-methoxyiminoa

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