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"6-(3-methoxyphenyl)-5,7-diphenyl-2,3,6,7-tetrahydropyrrolo[3,4-e][1,4]diazepin-8(1H)-one" is a complex organic compound with a molecular formula of C28H26N2O2. It features a pyrrolo[3,4-e][1,4]diazepine core, which is a fused ring system consisting of a pyrrole and a diazepine. The compound has a 6-(3-methoxyphenyl) substituent, indicating a methoxy group attached to a phenyl ring that is in turn attached to the core structure at the 6th position. Additionally, it has two phenyl groups attached at the 5th and 7th positions, contributing to its overall structure. 6-(3-methoxyphenyl)-5,7-diphenyl-2,3,6,7-tetrahydropyrrolo[3,4-e][1,4]diazepin-8(1H)-one is likely to be found in the realm of medicinal chemistry or as a synthetic intermediate due to its intricate structure and potential for biological activity.

5965-85-5

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5965-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5965-85-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,6 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5965-85:
(6*5)+(5*9)+(4*6)+(3*5)+(2*8)+(1*5)=135
135 % 10 = 5
So 5965-85-5 is a valid CAS Registry Number.

5965-85-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(3-methoxyphenyl)-5,7-diphenyl-1,2,3,6-tetrahydropyrrolo[3,4-e][1,4]diazepin-8-one

1.2 Other means of identification

Product number -
Other names Sulphuretin-triacetat

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5965-85-5 SDS

5965-85-5Downstream Products

5965-85-5Relevant academic research and scientific papers

Studies on Pitch Problems Caused by Pulping and Bleaching of Tropical Woods. XIV. Chemistry of the Aurone Derivatives at the Conventional Bleaching Stages

Ohtani, Yoshito,Sumimoto, Masashi

, p. 613 - 622 (2007/10/02)

Rengasin (1), which is responsible for the colored specks on a sheet of bleached sulfate pulp from the woods of rengas (Anacardiaceae), was converted into R1 7 having a novel carbon skeleton.A closely related analogue, S1 8, prepared from sulfuretin (2) was used as a model to investigate further conversions under bleaching conditions.Chlorination of S1 8 produced an equilibrium mixture involving compound 9 as a dominant compound.The latter was transformed by the treatment with chlorine dioxide into an orthoquinone (16) via two pathway containing 10 in one and 15 in another.The monomeric quinone (16) immediately dimerized in acidic media to give 20 under the same conditions as above, and the further oligomerization by the process similar to that in dimerization of 16 finally afforded a mixture of colored oligomers 26.

Carbon-13 Nmr Spectroscopy of Methoxy- and Acetoxyaurones

Sharma, Anil,Chibber, S. S.

, p. 275 - 277 (2007/10/02)

The 13C nmr chemical shifts of methoxy and acetoxyaurones are reported.The signals are assigned on the basis of substituent effects and comaprison with structurally related compounds.Assignments are also verified by Sford.

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