Cas 454709-85-4,Carbamic acid, (hexahydro-1H-1,4-diazepin-6-yl)-, 1,1-dimethylethyl ester

454709-85-4

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Basic information

Product Name: Carbamic acid, (hexahydro-1H-1,4-diazepin-6-yl)-, 1,1-dimethylethyl ester
Synonyms: Carbamic acid, (hexahydro-1H-1,4-diazepin-6-yl)-, 1,1-dimethylethyl ester
CAS NO:454709-85-4
Molecular Formula: C10H21N3O2
Molecular Weight: 215.29264
EINECS: N/A
Product Categories: N-BOC
Mol File: 454709-85-4.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 342.9±42.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.06±0.1 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 12.12±0.20(Predicted)
CAS DataBase Reference: Carbamic acid, (hexahydro-1H-1,4-diazepin-6-yl)-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, (hexahydro-1H-1,4-diazepin-6-yl)-, 1,1-dimethylethyl ester(454709-85-4)
EPA Substance Registry System: Carbamic acid, (hexahydro-1H-1,4-diazepin-6-yl)-, 1,1-dimethylethyl ester(454709-85-4)

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: 454709-85-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 454709-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,4,7,0 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 454709-85:
(8*4)+(7*5)+(6*4)+(5*7)+(4*0)+(3*9)+(2*8)+(1*5)=174
174 % 10 = 4
So 454709-85-4 is a valid CAS Registry Number.

454709-85-4Upstream product

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454709-85-4Relevant academic research and scientific papers

Radiolabeled Dibenzodiazepinone-Type Antagonists Give Evidence of Dualsteric Binding at the M2 Muscarinic Acetylcholine Receptor

Pegoli, Andrea,She, Xueke,Wifling, David,Hübner, Harald,Bernhardt, Günther,Gmeiner, Peter,Keller, Max

, p. 3314 - 3334 (2017)

The dualsteric ligand approach, aiming at ligands with improved subtype selectivity, has been increasingly applied to muscarinic receptors (MRs). In this article, we present the synthesis and characterization of a M2R subtype-preferring radiola

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