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103187-95-7

ETHYL 8-OXO-8-PHENYLOCTANOATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103187-95-7 Structure

  • Basic information

    1. Product Name: ETHYL 8-OXO-8-PHENYLOCTANOATE
    2. Synonyms: ETHYL 8-OXO-8-PHENYLOCTANOATE
    3. CAS NO:103187-95-7
    4. Molecular Formula: C16H22O3
    5. Molecular Weight: 262.34
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103187-95-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 368.515°C at 760 mmHg
    3. Flash Point: 159.633°C
    4. Appearance: /
    5. Density: 1.023g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.497
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: ETHYL 8-OXO-8-PHENYLOCTANOATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: ETHYL 8-OXO-8-PHENYLOCTANOATE(103187-95-7)
    12. EPA Substance Registry System: ETHYL 8-OXO-8-PHENYLOCTANOATE(103187-95-7)

  • 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: 103187-95-7(Hazardous Substances Data)

103187-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103187-95-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,1,8 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103187-95:
(8*1)+(7*0)+(6*3)+(5*1)+(4*8)+(3*7)+(2*9)+(1*5)=107
107 % 10 = 7
So 103187-95-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H22O3/c1-2-19-16(18)13-9-4-3-8-12-15(17)14-10-6-5-7-11-14/h5-7,10-11H,2-4,8-9,12-13H2,1H3

103187-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 8-OXO-8-PHENYLOCTANOATE

1.2 Other means of identification

Product number -
Other names ethyl 7-benzoylheptanoate

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:103187-95-7 SDS

103187-95-7Relevant articles and documents

(2-Amino-phenyl)-amides of ω-substituted alkanoic acids as new histone deacetylase inhibitors

Vaisburg, Arkadii,Bernstein, Naomy,Frechette, Sylvie,Allan, Martin,Abou-Khalil, Elie,Leit, Silvana,Moradei, Oscar,Bouchain, Giliane,Wang, James,Woo, Soon Hyung,Fournel, Marielle,Yan, Pu T.,Trachy-Bourget, Marie-Claude,Kalita, Ann,Beaulieu, Carole,Li, Zuomei,MacLeod, A. Robert,Besterman, Jeffrey M.,Delorme, Daniel

, p. 283 - 287 (2007/10/03)

A variety of ω-substituted alkanoic acid (2-amino-phenyl)-amides were designed and synthesized. These compounds were shown to inhibit recombinant human histone deacetylases (HDACs) with IC50 values in the low micromolar range and induce hyperacetylation of histones in whole cells. They induced expression of p21WAF1/Cip1 and caused cell-cycle arrest in human cancer cells. Compounds in this class showed efficacy in human tumor xenograft models.

Structurally simple trichostatin A-like straight chain hydroxamates as potent histone deacetylase inhibitors

Woo, Soon Hyung,Frechette, Sylvie,Khalil, Elie Abou,Bouchain, Giliane,Vaisburg, Arkadii,Bernstein, Naomy,Moradei, Oscar,Leit, Silvana,Allan, Martin,Fournel, Marielle,Trachy-Bourget, Marie-Claude,Li, Zuomei,Besterman, Jeffrey M.,Delorme, Daniel

, p. 2877 - 2885 (2007/10/03)

A series of new, structurally simple trichostatin A (TSA)-like straight chain hydroxamates were prepared and evaluated for their ability to inhibit partially purified human histone deacetylase 1 (HDAC-1). Some of these compounds such as 8m, 8n, 12, and 15

Inhibitors of histone deacetylase

-

, (2008/06/13)

The invention relates to the inhibition of histone deacetylase. The invention provides compounds and methods for inhibiting histone deacetylase enzymatic activity. The invention also provides compositions and methods for treating cell proliferative diseases and conditions.

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