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28362-76-7

Benzeneacetaldehyde, 2-ethyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 28362-76-7 Structure

  • Basic information

    1. Product Name: Benzeneacetaldehyde, 2-ethyl- (9CI)
    2. Synonyms: Benzeneacetaldehyde, 2-ethyl- (9CI);2-ethylBenzeneacetaldehyde
    3. CAS NO:28362-76-7
    4. Molecular Formula: C10H12O
    5. Molecular Weight: 148.20168
    6. EINECS: N/A
    7. Product Categories: PHENYL
    8. Mol File: 28362-76-7.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: Benzeneacetaldehyde, 2-ethyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzeneacetaldehyde, 2-ethyl- (9CI)(28362-76-7)
    11. EPA Substance Registry System: Benzeneacetaldehyde, 2-ethyl- (9CI)(28362-76-7)

  • 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: 28362-76-7(Hazardous Substances Data)

28362-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28362-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,6 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28362-76:
(7*2)+(6*8)+(5*3)+(4*6)+(3*2)+(2*7)+(1*6)=127
127 % 10 = 7
So 28362-76-7 is a valid CAS Registry Number.

28362-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-ethylphenyl)acetaldehyde

1.2 Other means of identification

Product number -
Other names Benzeneacetaldehyde,2-ethyl

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:28362-76-7 SDS

28362-76-7Relevant articles and documents

One-Pot Preparation of C1-Homologated Aliphatic Nitriles from Aldehydes through a Wittig Reaction under Metal-Cyanide-Free Conditions

Ezawa, Masatoshi,Togo, Hideo

, p. 2379 - 2384 (2017/05/01)

A one-pot protocol to obtain C1-homologated aliphatic nitriles was achieved by treating aromatic and aliphatic aldehydes with the (methoxymethyl)triphenylphosphonium ylide followed by hydrolysis of the resulting methyl vinyl ethers with pTsOH (Ts = para-toluenesulfonyl) and treatment with molecular iodine and aqueous ammonia under metal cyanide free conditions. Neopentyl-type nitriles, which could not be obtained by conventional methods that involved conversion of the neopentyl alcohol into a tosylate and treatment with metal cyanide, were successfully obtained by using the present method.

Synthesis and antiplasmodial activity of bicyclic dioxanes as simplified dihydroplakortin analogues

Gemma, Sandra,Kunjir, Sanil,Sanna Coccone, Salvatore,Brindisi, Margherita,Moretti, Vittoria,Brogi, Simone,Novellino, Ettore,Basilico, Nicoletta,Parapini, Silvia,Taramelli, Donatella,Campiani, Giuseppe,Butini, Stefania

, p. 5949 - 5953 (2011/10/09)

Here we report the synthesis and evaluation of antiplasmodial activity of a novel series of bicyclic peroxides inspired by the marine natural compound dihydroplakortin. We developed a synthetic strategy leading to the dihydroplakortin-related peroxides in only a few steps. The in vitro antiplasmodial potency of the peroxides was similar to, or greater than, that of the reference natural compound, and structure-activity relationship studies revealed several key structural requirements for activity and potency.

Furanyl, tetracyclic triterpene derivatives with immunosuppressant activity

-

, (2008/06/13)

The compounds of Formula I are useful as immunosuppressive agents.

Immunosuppressant tricyclic compounds

-

, (2008/06/13)

The compounds of Formula I are useful as immunosuppressive agents.

Tetracyclic triterpene derivatives with immunosuppressant activity

-

, (2008/06/13)

The compounds of Formula I are useful as immunosuppressive agents.

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