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1(3H)-Isobenzofuranone, 3-[4-(dimethylamino)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 62633-13-0 Structure
  • Basic information

    1. Product Name: 1(3H)-Isobenzofuranone, 3-[4-(dimethylamino)phenyl]-
    2. Synonyms:
    3. CAS NO:62633-13-0
    4. Molecular Formula: C16H15NO2
    5. Molecular Weight: 253.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 62633-13-0.mol
    9. Article Data: 2
  • 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: 1(3H)-Isobenzofuranone, 3-[4-(dimethylamino)phenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1(3H)-Isobenzofuranone, 3-[4-(dimethylamino)phenyl]-(62633-13-0)
    11. EPA Substance Registry System: 1(3H)-Isobenzofuranone, 3-[4-(dimethylamino)phenyl]-(62633-13-0)
  • 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: 62633-13-0(Hazardous Substances Data)

62633-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62633-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,3 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62633-13:
(7*6)+(6*2)+(5*6)+(4*3)+(3*3)+(2*1)+(1*3)=110
110 % 10 = 0
So 62633-13-0 is a valid CAS Registry Number.

62633-13-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[4-(dimethylamino)phenyl]-3H-2-benzofuran-1-one

1.2 Other means of identification

Product number -
Other names -

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:62633-13-0 SDS

62633-13-0Downstream Products

62633-13-0Relevant articles and documents

Near-infrared fluorophores containing benzo[c]heterocycle subunits

Meek, Scott T.,Nesterov, Evgueni E.,Swager, Timothy M.

supporting information; experimental part, p. 2991 - 2993 (2009/05/07)

(Chemical Equation Presented) The syntheses and spectroscopic properties of eight new push-pull-type near-infrared fluorophores that contain either isobenzofuran or isothianaphthene subunits are presented. The isobenzofuran dyes demonstrate significantly red-shifted absorption compared with their isothianaphthene counterparts, which is attributed to isobenzofuran's more potent pro-quinoidal character.

Isoindolin-1-one derivative and antiarrhythmic agent

-

, (2008/06/13)

Isoindolin-1-one compounds represented by the following formula (I); STR1 {wherein n represents an integer of 1 to 6; m represents 0 or 1; R1, R2 and R3 are each independently hydrogen or lower alkyl, and when m is 1, R1 and one of R2 and R3 may form a five-membered or six-membered ring over N atom; X represents hydrogen or hydroxy; Ar represents naphthyl, pyridyl or substituted phenyl represented by the formula (II); Ar and X may form a lactone ring; STR2 [wherein Y represents carboxyl, lower alkoxycarbonyl, carbamoyl, N,N-lower alkyl-substituted carbamoyl or amino represented by the formula (III): STR3 (wherein R6 and R7 are each independently hydrogen, lower alkyl or lower alkanoyl); R4 and R5 are each independently hydrogen, lower alkyl, cyano or halogen]} or a pharmaceutically acceptable acid addition salt or metal salt thereof have an excellent antiarrhythmic activity.

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