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150681-19-9

Benzamide, 2-methyl-N-[4-[(2,3,4,5-tetrahydro-5-hydroxy-1H-1-benzazepin-1-yl)carb onyl]phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 150681-19-9 Structure

  • Basic information

    1. Product Name: Benzamide, 2-methyl-N-[4-[(2,3,4,5-tetrahydro-5-hydroxy-1H-1-benzazepin-1-yl)carb onyl]phenyl]-
    2. Synonyms:
    3. CAS NO:150681-19-9
    4. Molecular Formula: C25H24N2O3
    5. Molecular Weight: 400.477
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 150681-19-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzamide, 2-methyl-N-[4-[(2,3,4,5-tetrahydro-5-hydroxy-1H-1-benzazepin-1-yl)carb onyl]phenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzamide, 2-methyl-N-[4-[(2,3,4,5-tetrahydro-5-hydroxy-1H-1-benzazepin-1-yl)carb onyl]phenyl]-(150681-19-9)
    11. EPA Substance Registry System: Benzamide, 2-methyl-N-[4-[(2,3,4,5-tetrahydro-5-hydroxy-1H-1-benzazepin-1-yl)carb onyl]phenyl]-(150681-19-9)

  • 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: 150681-19-9(Hazardous Substances Data)

150681-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150681-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,6,8 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 150681-19:
(8*1)+(7*5)+(6*0)+(5*6)+(4*8)+(3*1)+(2*1)+(1*9)=119
119 % 10 = 9
So 150681-19-9 is a valid CAS Registry Number.

150681-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-1-[4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-1-benzazepine

1.2 Other means of identification

Product number -
Other names N-[4-(5-Hydroxy-2,3,4,5-tetrahydro-benzo[b]azepine-1-carbonyl)-phenyl]-2-methyl-benzamide

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:150681-19-9 SDS

150681-19-9Relevant articles and documents

Tolvaptan-Type Vasopressin Receptor Ligands: Important Role of Axial Chirality in the Active Form

Tabata, Hidetsugu,Yoneda, Tetsuya,Oshitari, Tetsuta,Takahashi, Hideyo,Natsugari, Hideaki

, p. 4503 - 4509 (2017/06/05)

The anti and syn isomers of tolvaptan-type compounds, N-benzoyl-5-hydroxy-1-benzazepines (5a-c), were prepared in a stereocontrolled manner by biasing the conformation with a methyl group at C9 and C6, respectively, and the enantiomeric forms were separat

Orally active, nonpeptide vasopressin V2 receptor antagonists: A novel series of 1-[4-(benzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepines and related compounds

Ogawa, Hidenori,Yamashita, Hiroshi,Kondo, Kazumi,Yamamura, Yoshitaka,Miyamoto, Hisashi,Kan, Keizo,Kitano, Kazuyoshi,Tanaka, Michinori,Nakaya, Kenji,Nakamura, Shigeki,Mori, Toyoki,Tominaga, Michiaki,Yabuuchi, Youichi

, p. 3547 - 3555 (2007/10/03)

This paper describes a novel series of nonpeptide vasopressin V2 receptor antagonists. It has been demonstrated that the 1-[4- (benzoylamino)benzoyl]-2,3,4,5-1H-benzazepines and 1-[4- (benzoylamino)benzoyl]-2,3,4,5-1H-1,5-benzodiazepines show a high affinity for V2 (and V(1a)) receptors. Among the 1-[4-(benzoylamino)benzoyl]-2,3,4,5- 1H-benzazepine series, compounds with an alkylamino group on the benzazepine ring have been shown to have oral activity. A lipophilic group at the ortho position on the terminal benzoyl ring is important for both high V2 receptor affinity and oral activity. On the basis of these favorable properties, clinical testing of 31b has begun for use as an oral and iv aquaretic agent.

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