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14811-68-8

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14811-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14811-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,1 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14811-68:
(7*1)+(6*4)+(5*8)+(4*1)+(3*1)+(2*6)+(1*8)=98
98 % 10 = 8
So 14811-68-8 is a valid CAS Registry Number.

14811-68-8SDS

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 3-methyl-5-oxo-5-[2]thienyl-valeric acid methyl ester

1.2 Other means of identification

Product number -
Other names 3-Methyl-5-oxo-5-[2]thienyl-valeriansaeure-methylester

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:14811-68-8 SDS

14811-68-8Relevant articles and documents

Design, Synthesis, and Evaluation of ω-Iodovinyl- and ω-Iodoalkyl-Substituted Methyl Branched Long Chain Fatty Acids

Goodman, Mark M.,Callahan, A. P.,Knapp, F. F.

, p. 807 - 815 (1985)

The synthesis of a new methyl-branched fatty acid, (E)-19-iodo-3(RS)-methyl-18-nonadecenoic acid (19), is described.Methyl branching has been introduced at the 3 position to inhibit β-oxidation and radioiodide has been attached as a trans-vinyl iodide.Preparation of 19 involved a 15-step sequence of reactions climaxing with formation of the methyl ester 18 by iododestannylation of methyl (E)-19-(tri-n-butylstannyl)-3(RS)-methyl-18-nonadecenoate (17) resulting from the reaction of n-Bu3SnH with methyl 3(RS)-methyl-18-nonadecynoate (16).Methyl branching was introduced at an early stage by Friedl-Crafts acylation of thiophene with 3(RS)-methyl-4-carbomethoxybutanoyl chloride (3) generated from 3-methylglutaric anhydride.The new agent -19, showed high myocardial uptake (5 min, 4.89percent dose/g; 30 min, 3.32percent dose/g), good heart/blood (H/B) ratios (5 min, 5.4/1; 30 min, 4.3/1), and significantly greater myocardial retention in fasted rats than the corresponding straight-chain analogue 19-iodo-18-nonadecenoic acid (5 min, 3.52percent dose/g, H/B = 4.8/1; 30 min, 1.19percent dose/g, H/B = 1.6/1).Excellent myocardial images were obtained in rats after administration of -19 and confirmed the slow myocardial washout over a 60-min period.These data suggest that 19 is a good candidate for evaluation of heart disease involving aberrations in fatty acid metabolism by use of imaging techniques such as single photon emission computerized tomography (SPECT) where redistribution or washout should be minimized.

SYNTHESIS OF MACROCYCLIC COMPOUNDS 21. PREPARATION, CONFORMATIONAL BEHAVIOR, AND REDUCTIVE DESULFURIZATION OF 8-METHYL-2,3-BENZO-5-OXA-α-CYCLOTHIEN-1,4-DIONE

Alashev, F. D.,Bulgakova, V. N.,Taits, S. Z.,Gol'dfarb, Ya. L.

, p. 990 - 994 (2007/10/02)

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