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3,5-DiMethyl-4-nitrobenzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 18515-18-9 Structure
  • Basic information

    1. Product Name: 3,5-DiMethyl-4-nitrobenzaldehyde
    2. Synonyms: 3,5-DiMethyl-4-nitrobenzaldehyde
    3. CAS NO:18515-18-9
    4. Molecular Formula: C9H9NO3
    5. Molecular Weight: 179.17266
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 18515-18-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,5-DiMethyl-4-nitrobenzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-DiMethyl-4-nitrobenzaldehyde(18515-18-9)
    11. EPA Substance Registry System: 3,5-DiMethyl-4-nitrobenzaldehyde(18515-18-9)
  • 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: 18515-18-9(Hazardous Substances Data)

18515-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18515-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,1 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18515-18:
(7*1)+(6*8)+(5*5)+(4*1)+(3*5)+(2*1)+(1*8)=109
109 % 10 = 9
So 18515-18-9 is a valid CAS Registry Number.

18515-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethyl-4-nitrobenzaldehyde

1.2 Other means of identification

Product number -
Other names 3,5-dimethyl-4-nitro-benzaldehyde

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:18515-18-9 SDS

18515-18-9Relevant articles and documents

FRET studies on a series of BODIPY-dye-labeled switchable resorcin[4]arene cavitands

Pochorovski, Igor,Breiten, Benjamin,Schweizer, W. Bernd,Diederich, Francois

, p. 12590 - 12602 (2010)

A series of borondipyrromethane (BODIPY)-dye-labeled resorcin[4]arene cavitands 1-4 with different lengths of oligo(phenylene-ethynylene) spacers between the dyes and the macrocyclic rim has been synthesized. Their switching behavior from the "vase" to "k

Novel metal oxide nanocomposite of Au/CuO-ZnO for recyclable catalytic aerobic oxidation of alcohols in water

Albadi, Jalal,Alihoseinzadeh, Amir,Razeghi, Abdolhosein

, p. 1 - 5 (2014/03/21)

CuO-ZnO supported gold nanoparticle is introduced as a new, efficient, and recyclable catalyst for the aerobic oxidation of alcohols. The CuO-ZnO support was prepared by co-precipitation and Au nanoparticles were loaded on support by a deposition-precipitation method. The catalyst was characterized by XRD, BET surface area, FESEM, EDS and HRTEM techniques. A wide range of alcohols, including benzylic, primary and secondary alcohols are converted into the corresponding carbonyl derivatives. The experimental procedure with Au/CuO-ZnO catalyst is quite straightforward and the catalyst is recyclable up to 6 consecutive runs by simple filtration.

NOVEL ACYLAMINOBENZAMIDE DERIVATIVES

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Page/Page column 75, (2010/04/03)

The present invention relates to novel Acylaminobenzamide derivatives represented by the following formula (I) and use thereof as pesticides: wherein V represents an aromatic ring group of V1 to V5 described in the detailed description, Q represents an ar

HIV INHIBITING 1,2,4-TRIAZINES

-

Page 46, (2008/06/13)

The present invention relates to HIV replication inhibitors of formula (I) as defined in the specification their use as a medicine, their processes for preparation and pharmaceutical compositions comprising them.

Migrations in Oxidations of Mesidine

Goldstein, Stephen L.,McNelis, Edward

, p. 1613 - 1620 (2007/10/02)

The oxidation of mesidine in methanolic media by ferricyanide, dichromate, and persulfate afforded an anil 4 containing a shifted methoxymethyl group in addition to the principal anil 3 formed by oxidative dealkylation.Possible intermediates 6, 7, and 8 were prepared and oxidized to the product anils.Oxidations of related anilines 9, 10, and 13 did not parallel those of mesidine but afforded analogues of 3.There is significant spectral evidence for anils with alkyl shifts but little for anils analogous to 4.

Comparative Reactivity of Substituted 4-Nitrobenzylidene Dichlorides with Alkali

Goh, Swee Hock,Kam, Toh Seok

, p. 423 - 426 (2007/10/02)

A comparative study of the reactions of substituted 4-nitrobenzylidene dichlorides ArCHCl2 (Ar = 3-Cl-4-NO2C6H3, 2-Cl-4-NO2C6H3, 4-NO2C6H4, 3,5-Me2-4-NO2C6H2, and 2-Me-4-NO2C6H3) with aqueous alcoholic alkali shows that chlorine substitution enhances the

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