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5-chloro-2-methyl-1H-isoindole-1,3(2H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 63197-17-1 Structure
  • Basic information

    1. Product Name: 5-chloro-2-methyl-1H-isoindole-1,3(2H)-dione
    2. Synonyms: 1H-isoindole-1,3(2H)-dione, 5-chloro-2-methyl-; 5-Chloro-2-methyl-1H-isoindole-1,3(2H)-dione
    3. CAS NO:63197-17-1
    4. Molecular Formula: C9H6ClNO2
    5. Molecular Weight: 195.6024
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63197-17-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 315.5°C at 760 mmHg
    3. Flash Point: 144.6°C
    4. Appearance: N/A
    5. Density: 1.454g/cm3
    6. Vapor Pressure: 0.000435mmHg at 25°C
    7. Refractive Index: 1.619
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 5-chloro-2-methyl-1H-isoindole-1,3(2H)-dione(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-chloro-2-methyl-1H-isoindole-1,3(2H)-dione(63197-17-1)
    12. EPA Substance Registry System: 5-chloro-2-methyl-1H-isoindole-1,3(2H)-dione(63197-17-1)
  • 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: 63197-17-1(Hazardous Substances Data)

63197-17-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63197-17-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,9 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63197-17:
(7*6)+(6*3)+(5*1)+(4*9)+(3*7)+(2*1)+(1*7)=131
131 % 10 = 1
So 63197-17-1 is a valid CAS Registry Number.

63197-17-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-2-methylisoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 5-chloro-2-methyl-isoindole-1,3-dione

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:63197-17-1 SDS

63197-17-1Relevant articles and documents

Two new isomerous fluorescent chemosensors for Al3+ based on photoinduced electron transfer

Jiang, Xiu-Juan,Tang, Hao,Li, Xiao-Yuan,Zang, Shuang-Quan,Hou, Hong-Wei,Mak, Thomas C.W.

, p. 26 - 32 (2013)

Two new isomerous PET fluorescent chemosensors (L and L') for Al 3+ have been designed, synthesized and characterized. The two chemosensors exhibited fluorescence enhancement upon binding Al3+ in CH3-CN by PET inhibition processes from both the sulfur and the nitrogen donors to anthracene. The job's plot, Benesi-Hildebrand plot and 1H NMR titration experiments indicate that both chemosensors form a 1: 1 complex with Al3+. The binding constants were calculated to be (1.432 ±0.186) × 105 and (1.427 ± 0.970) × 105, respectively. Furthermore, the lowest detection limit for Al3+ in CH3CN was determined to be 4.8 × 10 7 M and 2.2 × 10 7 M, respectively.

NOVEL COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

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Paragraph 0419-0422, (2019/10/29)

The present invention relates to a novel compound capable of improving efficiency and low driving voltage and/or lifespan characteristics in an organic light emitting device; and an organic light emitting device including the same. The compound is represe

Isoindol - 1, 3 - dione compound and its preparation method and application (by machine translation)

-

, (2017/08/02)

The invention discloses a isoindole - 1, 3 - dione compound and its preparation method and application. The general formula (I) has the structure shown. The invention of the isoindole - 1, 3 - diones to LNCap cells with cell inhibitory activity, can be used for preparing anti-tumor drug. (by machine translation)

Photophysical properties of ESIPT inspired fluorescent 2-(2-hydroxyphenyl)- 6-methylimidazo[4,5-f]isoindole-5,7(1H,6H)-dione and its derivative: Experimental and DFT based approach

Deshmukh, Mininath S.,Sekar, Nagaiyan

, p. 457 - 465 (2014/12/11)

The excited-state intramolecular proton transfer chromophores 2-(2-hydroxyphenyl)-6-methylimidazo[4,5-f]isoindole-5,7(1H,6H)-dione and 2-(4-(diethylamino)-2-hydroxyphenyl)-6-methylimidazo[4,5-f]isoindole-5,7(1H,6H) -dione are synthesized from 4,5-diamino-

PREPARATION OF SUBSTITUTED PHTHALIC ANHYDRIDE, ESPECIALLY 4-CHLOROPHTALIC ANHYDRIDE

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Page 7, (2008/06/13)

A method for the synthesis of substituted phthalic anhydrides (IV) wherein R' is a halogen, aromatic or aliphatic group comprising 1-18 carbons, hydrogen or nitro group is the transimidation between a substituted N-alkyl phthalimide (V) wherein R is an alkyl having from 1 to 18 carbons, and a substituted tetrahydrophthalic anhydride (VI): The by product of this reaction, a substituted N-alkyl tetrahydrophthalimide (VII), may be converted by aromatization to the substituted N-alkyl phthalimide (V).

Methods for the preparation of 4-chlorophthalic anhydride

-

, (2008/06/13)

A method for the synthesis of substituted phthalic anhydrides (IV)wherein R' is a halogen, aromatic or aliphatic group comprising 1-18 carbons, hydrogen or nitro group is the transimidation between a substituted N-alkyl phthalimide (V)wherein R is an alkyl having from 1 to 18 carbons, and a substituted tetrahydrophthalic anhydride (VI):The by-product of this reaction, a substituted N-alkyl tetrahydrophthalimide (VII), may be converted by aromatization to the substituted N-alkyl phthalimide (V).

On the Reaction of α-Chlorobenzylic Cations with Isocyanates

Ismail, A. El-Hamid,Hamed, A.,Abdel-Aal, M. Taha,Zeid, I.,Al-Talib, M.,et al.

, p. 661 - 668 (2007/10/02)

Isocyanates react as N-nucleophiles with α-chlorobenzylic cations (2) to give 1-oxoisoindolium salts (5).From the reaction of benzotrichlorides with SbCl5 and isocyanates the extremely reactive hexachloroantimonates 5 with R2=Cl are isolated.Hydrolysis of these cyclic N-acyl iminium salts affords phthalimides 6.Reaction of 5k with dimethylcyanamide gives the 2-azoniaallene salt 13. p-Tolyl isocyanate is Friedel-Crafts alkylated by p-chlorobenzotrichloride (1i) in the presence of SbCl5 to furnish the 1,3-oxadiazonium salt 7, which is hydrolyzed to give the benzophenone 9.With ethanol the acetals 10 and 11 are formed from 7.

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