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Propanedioic acid, [(3,5-dimethylphenyl)methyl]methyl-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52528-74-2

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52528-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52528-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,2 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52528-74:
(7*5)+(6*2)+(5*5)+(4*2)+(3*8)+(2*7)+(1*4)=122
122 % 10 = 2
So 52528-74-2 is a valid CAS Registry Number.

52528-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-[(3,5-dimethylphenyl)methyl]-2-methylpropanedioate

1.2 Other means of identification

Product number -
Other names Propanedioic acid,[(3,5-dimethylphenyl)methyl]methyl-,diethyl ester

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:52528-74-2 SDS

52528-74-2Relevant academic research and scientific papers

Studies in Terpenoids: Part LXI - Synthesis of (+/-)-Pterosin-B

John, T. K.,Angadi, V. B.,Rao, Krishna G. S.

, p. 735 - 737 (2007/10/02)

(+/-)-Pterosin-B (1), a sesquiterpene constituent of several ferns, has been synthesized in excellent yield by the regiospecific oxidation of the diol (12) obtained by LAH reduction of the dihydroderivatives (10 and 11) of (+/-)-pterosin-E (2).

Carbon-13 Nuclear Magnetic Resonance Spectra of Pterosin-Sesquiterpenes and Related Indan-1-one Derivatives

Fukuoka, Masamichi,Yoshihira, Kunitoshi,Natori, Shinsaku,Mihashi, Kunihide,Nishi, Masatoshi

, p. 3113 - 3128 (2007/10/02)

Methyl derivatives of indan-1-one were prepared as models to aid in interpreting the carbon-13 nuclear magnetic resonance ((13)C-NMR) spectra of pterosin-sesquiterpenes which were isolated from bracken fern, Pteridium aquilinum var. latiusculum.The chemical shifts of the carbons of the methylindan-1-ones were assigned by the proton decoupling technique.All the (13)C-NMR signals of the pterosin-sesquiterpenes were assigned by means of selective proton decouplings, and from the (13)C-(1)H long-range couplings and (13)C chemical shifts of the model compounds.Keywords - indan-1-one derivative; methylindan-1-one; pterosin-sesquiterpene; methylindan-1-one synthesis; (1)H-NMR; (13)C-NMR; selective decoupling; C-H decoupling

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