Cas 104769-65-5,3-(3-Hydroxy-propyl)-1-methoxymethyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione

104769-65-5

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Basic information

Product Name: 3-(3-Hydroxy-propyl)-1-methoxymethyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione
Synonyms:
CAS NO:104769-65-5
Molecular Formula:
Molecular Weight: 278.308
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: 3-(3-Hydroxy-propyl)-1-methoxymethyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione(CAS DataBase Reference)
NIST Chemistry Reference: 3-(3-Hydroxy-propyl)-1-methoxymethyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione(104769-65-5)
EPA Substance Registry System: 3-(3-Hydroxy-propyl)-1-methoxymethyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione(104769-65-5)

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: 104769-65-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 104769-65-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,6 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104769-65:
(8*1)+(7*0)+(6*4)+(5*7)+(4*6)+(3*9)+(2*6)+(1*5)=135
135 % 10 = 5
So 104769-65-5 is a valid CAS Registry Number.

104769-65-5Upstream product

104769-63-3 10-Methoxymethyl-1,11a-dihydro-2H,10H-benzo[e]pyrrolo[1,2-a][1,4]diazepine-3,5,11-trione

104769-65-5Downstream Products

104769-65-5Relevant academic research and scientific papers

A ONE STEP SYNTHESIS OF 1,4-BENZODIAZEPINES:SYNTHETIC STUDIES ON NEOTHRAMYCIN

Mori, Miwako,Kimura, Masaya,Uozumi, Yasuhiro,Ban, Yoshio

, p. 5947 - 5950 (2007/10/02)

A one step synthesis of 1,4-benzodiazepines from o-haloanilines and amino acids was achieved by use of palladium catalyzed carbonylation, by which application a synthesis of the model compounds (23a and 23b) of Neothramycin (A and B) was described.An efficient chemoselective reduction of the amide was provided.

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