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102626-21-1

1,3-Benzenedicarboxaldehyde, 4-chloro-5-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 102626-21-1 Structure

  • Basic information

    1. Product Name: 1,3-Benzenedicarboxaldehyde, 4-chloro-5-methyl-
    2. Synonyms:
    3. CAS NO:102626-21-1
    4. Molecular Formula: C9H7ClO2
    5. Molecular Weight: 182.606
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102626-21-1.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: 1,3-Benzenedicarboxaldehyde, 4-chloro-5-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Benzenedicarboxaldehyde, 4-chloro-5-methyl-(102626-21-1)
    11. EPA Substance Registry System: 1,3-Benzenedicarboxaldehyde, 4-chloro-5-methyl-(102626-21-1)

  • 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: 102626-21-1(Hazardous Substances Data)

102626-21-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102626-21-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,6,2 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 102626-21:
(8*1)+(7*0)+(6*2)+(5*6)+(4*2)+(3*6)+(2*2)+(1*1)=81
81 % 10 = 1
So 102626-21-1 is a valid CAS Registry Number.

102626-21-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-5-methylbenzene-1,3-dicarbaldehyde

1.2 Other means of identification

Product number -
Other names chloro-6-methylbenzene-2,4-dicarboxaldehyde

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:102626-21-1 SDS

102626-21-1Downstream Products

102626-21-1Relevant articles and documents

A novel one-step conversion of α,β-epoxy ketones to o-dichlorobenzaldehydes by the Vilsmeier reaction

Megati, Sreenivasulu,Rao, Krishna G. S.

, p. 5819 - 5822 (2007/10/02)

A novel, versatile one-step synthesis of o-dichlorobenzaldehydes has been developed. Acyclic α,β-epoxy ketones undergo the Vilsmeier reaction to afford o-dichlorobenzenemono- and dicarboxyaldehydes whereas cyclic α,β-epoxy ketones gave des and chlorobenzenedicarboxyaldehydes.

Vilsmeier reaction studies on some α,β-unsaturated alkenones

Sreenivasulu, M.,Rao, G. S. Krishna

, p. 494 - 495 (2007/10/02)

α,β-Unsaturated alkenones (1a-g) are converted into chlorobenzenemono-, di- and tricarboxaldehydes (2a-h) under Vilsmeier reaction conditions.Besides six known chlorobenzaldehydes the route affords, in a one-pot reaction, two new members of this class of compounds, 3-methyl-(2d) and 3,5-dimethyl-(2h)-2-chlorobenzaldehydes.

Chlorobenzenedicarboxaldehyde and Chlorobenzenetricarboxaldehyde from Cyclohexenones under Vilsmeier Reaction Conditions

Raju, B.,Rao, G. S. Krishna

, p. 177 - 178 (2007/10/02)

The isomeric cyclohexenone mixture (II+III), (VI+VII) and (X+XI) afford on Vilsmeier reaction the chlorobenzenecarboxaldehydes (IV), (VIII) and (XII), respectively in good yields.Besi

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