Cas 1259320-89-2,10-benzyl-11a-chlorobenzo[e]oxazolo[3,2-a][1,4]-diazepine-2,3,5,11(10H,11aH)-tetraone

1259320-89-2

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Basic information

Product Name: 10-benzyl-11a-chlorobenzo[e]oxazolo[3,2-a][1,4]-diazepine-2,3,5,11(10H,11aH)-tetraone
Synonyms: 10-benzyl-11a-chlorobenzo[e]oxazolo[3,2-a][1,4]-diazepine-2,3,5,11(10H,11aH)-tetraone
CAS NO:1259320-89-2
Molecular Formula:
Molecular Weight: 370.749
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: 10-benzyl-11a-chlorobenzo[e]oxazolo[3,2-a][1,4]-diazepine-2,3,5,11(10H,11aH)-tetraone(CAS DataBase Reference)
NIST Chemistry Reference: 10-benzyl-11a-chlorobenzo[e]oxazolo[3,2-a][1,4]-diazepine-2,3,5,11(10H,11aH)-tetraone(1259320-89-2)
EPA Substance Registry System: 10-benzyl-11a-chlorobenzo[e]oxazolo[3,2-a][1,4]-diazepine-2,3,5,11(10H,11aH)-tetraone(1259320-89-2)

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: 1259320-89-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1259320-89-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,9,3,2 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1259320-89:
(9*1)+(8*2)+(7*5)+(6*9)+(5*3)+(4*2)+(3*0)+(2*8)+(1*9)=162
162 % 10 = 2
So 1259320-89-2 is a valid CAS Registry Number.

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1259320-89-2Relevant academic research and scientific papers

Cyclic Oxalylation of Primary N-Substituted Anthranilamides: 1H-Benzoe]1, 4]diazepine-2, 3, 5(4H)-triones and 11a-Chlorobenzoe]oxazolo3, 2-a]1, 4]diazepine-2, 3, 5, 11(10H, 11aH)-tetraones

Koellner, Maria Anna,Geffken, Detlef

experimental part, p. 1155 - 1160 (2011/01/08)

In dependence on the molar ratio, the reaction of primary anthranilamides 3 with oxalyl chloride produced 1H-benzoe]1,4]diazepine-2,3,5(4H)-triones 4 or 10-substituted 11a-chloro-benzoe]-oxazolo3,2-a]1,4]diazepine-2,3,5,11(10H, 11aH)-tetraones 5, the stru

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