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CAS

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169758-66-1

Robalzotan is a compound with specific properties that make it suitable for various applications across different industries. It is characterized by its unique chemical structure and functional groups that allow it to interact with other molecules and systems.

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  • 2H-1-Benzopyran-5-carboxamide,3-(dicyclobutylamino)-8-fluoro-3,4-dihydro-, (3R)-

    Cas No: 169758-66-1

  • USD $ 1.9-2.9 / Gram

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  • 169758-66-1 Structure

  • Basic information

    1. Product Name: Robalzotan
    2. Synonyms: Robalzotan;Robalzotan [inn];Unii-I18m56ogme;(3R)-3-(Dicyclobutylamino)-8-fluoro-3,4-dihydro-2H-1-benzopyran-5-carboxamidehydrochloride;NAD 299;(R)-3-(DicyclobutylaMino)-8-fluorochroMan-5-carboxaMide;NAD 299 hydrochloride (Robalzotan);NAD 299 hydrochloride
    3. CAS NO:169758-66-1
    4. Molecular Formula: C18H23FN2O2.C4H6O6.H2O
    5. Molecular Weight: 486.49
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 169758-66-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 429.9°C at 760 mmHg
    3. Flash Point: 213.8°C
    4. Appearance: /
    5. Density: 1.27g/cm3
    6. Vapor Pressure: 1.36E-07mmHg at 25°C
    7. Refractive Index: 1.603
    8. Storage Temp.: Desiccate at RT
    9. Solubility: N/A
    10. PKA: 15.72±0.40(Predicted)
    11. CAS DataBase Reference: Robalzotan(CAS DataBase Reference)
    12. NIST Chemistry Reference: Robalzotan(169758-66-1)
    13. EPA Substance Registry System: Robalzotan(169758-66-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 169758-66-1(Hazardous Substances Data)

169758-66-1 Usage

Uses

Used in Psychotropic Drug Development:
Robalzotan is used as a selective, high affinity 5-HT1A antagonist for the development of psychotropic drugs. Its ability to modulate serotonin receptors plays a crucial role in addressing various psychiatric and neurological conditions.
If there are additional applications in different industries, they can be listed as follows:
Used in [Application Industry]:
Robalzotan is used as [application type] for [application reason].
Please provide more information or context about the specific applications and industries for Robalzotan, and I can help you organize the description and uses accordingly.

Biological Activity

Selective, high affinity 5-HT 1A receptor antagonist (K i = 0.6 nM in vitro ).

Check Digit Verification of cas no

The CAS Registry Mumber 169758-66-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,7,5 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 169758-66:
(8*1)+(7*6)+(6*9)+(5*7)+(4*5)+(3*8)+(2*6)+(1*6)=201
201 % 10 = 1
So 169758-66-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H23FN2O2/c19-16-8-7-14(18(20)22)15-9-13(10-23-17(15)16)21(11-3-1-4-11)12-5-2-6-12/h7-8,11-13H,1-6,9-10H2,(H2,20,22)/t13-/m1/s1

169758-66-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R)-3-[di(cyclobutyl)amino]-8-fluoro-3,4-dihydro-2H-chromene-5-carboxamide

1.2 Other means of identification

Product number -
Other names Robalzotan

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:169758-66-1 SDS

169758-66-1Downstream Products

169758-66-1Relevant articles and documents

Process for the manufacture of 3-N-N-dicyclobutylamino-8-fluoro-3, 4-dihydro-2H-1-benzopyran-5-carboxamide

-

, (2008/06/13)

A process for the manufacture of the racemic compound of the formula (I), its R-enantiomer (formula R-(I)) and its S-enantiomer (formula S-(I)), and pharmaceutically acceptable salts and/or solvates thereof, as well as new intermediates obtained and used in the process.

Combination of 5-HT uptake inhibitor with a selective 5-HT1A antagonist

-

, (2008/06/13)

The invention relates to a combination of a first component (a) which is a 5-HT reuptake inhibitor and a second component (b) which is selective 5-HT 1A antagonist of the general formula wherein R 1 is n-propyl or cyclobutyl; R 2 is isopropyl, tertiary bu

USE OF 5-HT1A RECEPTOR ANTAGONISTS FOR THE TREATMENT OF URINARY INCONTINENCE

-

, (2008/06/13)

The present invention discloses compositions and methods for treating neuromuscular dysfunction of the lower urinary tract in mammals, including humans, using serotonin 5-HT 1A receptor antagonist compounds that exert their inhibitory effects via pre-syna

(R)-5-CARBAMOYL-8-FLUORO-3-N,N-DISUBSTITUTED-AMINO-3,4-DIHYDRO-2H-1-BENZOPYRANS

-

, (2008/06/13)

Compounds of the general formula STR1 wherein R 1 is n-propyl or cyclobutyl;R 2 is isopropyl, tertiary butyl, cyclobutyl, cyclopentyl or cyclohexyl;R 3 is hydrogen;R 4 is hydrogen or methyl;as (R)-enantiomer in the form of free ba

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