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CHEMBRDG-BB 9071633 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93189-07-2 Structure
  • Basic information

    1. Product Name: CHEMBRDG-BB 9071633
    2. Synonyms: CHEMBRDG-BB 9071633;3-(ANILINOMETHYL)PHENOL;UKRORGSYN-BB BBV-118836;3-(anilinomethyl)phenol(SALTDATA: FREE)
    3. CAS NO:93189-07-2
    4. Molecular Formula: C13H13NO
    5. Molecular Weight: 199.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93189-07-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 374.3°C at 760 mmHg
    3. Flash Point: 163.3°C
    4. Appearance: /
    5. Density: 1.185g/cm3
    6. Vapor Pressure: 3.92E-06mmHg at 25°C
    7. Refractive Index: 1.662
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: CHEMBRDG-BB 9071633(CAS DataBase Reference)
    11. NIST Chemistry Reference: CHEMBRDG-BB 9071633(93189-07-2)
    12. EPA Substance Registry System: CHEMBRDG-BB 9071633(93189-07-2)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 93189-07-2(Hazardous Substances Data)

93189-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93189-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,8 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93189-07:
(7*9)+(6*3)+(5*1)+(4*8)+(3*9)+(2*0)+(1*7)=152
152 % 10 = 2
So 93189-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO/c15-13-8-4-5-11(9-13)10-14-12-6-2-1-3-7-12/h1-9,14-15H,10H2

93189-07-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(anilinomethyl)phenol

1.2 Other means of identification

Product number -
Other names m-hydroxybenzyl aniline

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:93189-07-2 SDS

93189-07-2Relevant articles and documents

Transfer hydrogenation of aldehydes and ketones catalyzed using an aminophosphinite POCNHpincer complex of Ni(ii)

?ztop?u, ?zgür,Hayrapetyan, Davit,Khalimon, Andrey Y.,Lyssenko, Konstantin A.,Segizbayev, Medet,Shakhman, Dinmukhamed

, p. 11950 - 11957 (2020/09/21)

The aminophosphinite pincer complex (POCNH)NiBr was found to effectively catalyze the transfer hydrogenation of aldehydes and ketones with 2-propanol and KOtBu as a base, presenting a rare example of bifunctional nickel transfer hydrogenation catalysts. The transfer hydrogenation of aldehydes and ketones was found to be selective, tolerating a wide range of other functional groups, including those prone to reduction, such as esters, amides, alkenes, pyridines, and nitriles. The reactions were suggested to proceedviathe metal-ligand cooperative mechanism with an intermediacy of an amido (POCN)NiIIspecies.

NOVEL COMPOUNDS

-

Page/Page column, (2014/06/23)

Compounds of formula (I) described herein are inhibitors of the phosphodiesterase 4 (PDE4) enzyme and muscarinic M3 receptor antagonists and are useful for the prevention and/or treatment of diseases of the respiratory tract characterized by airway obstru

4-amino-thieno[3,2-c] pyridine-7-carboxylic acid derivatives

-

Page/Page column 39, (2010/11/26)

The present invention relates to compounds of the formula medicaments containing them and the use of these compounds as pharmaceutically active agents. The compounds exhibit activity as Raf kinase inhibitors and therefore may be useful for the treatment of diseases mediated by said kinases, especially as anticancer agents.

Thiourea-catalyzed transfer hydrogenation of aldimines

Zhang, Zhiguo,Schreiner, Peter R.

, p. 1455 - 1457 (2008/03/11)

The present letter reports on the thiourea-catalyzed transfer hydrogenation of imines through hydrogen-bonding activation with Hantzsch 1,4-dihydropyridine as the hydrogen source. A variety of aromatic as well as aliphatic aldimines can be reduced to give

Method of topically treating inflammation

-

, (2008/06/13)

This invention describes a method of treating inflammation in warmblooded animals by topically administering an effective amount of benzylamine and its derivatives.

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