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80683-81-4

80683-81-4

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80683-81-4 Usage

Type of compound

Organic compound

Structure

Long carbon chain with a sulfide functional group and a carboxylic acid group

Applications

a. Production of fragrances
b. Production of flavors
c. Pharmaceutical industry
d. Intermediate in the synthesis of other organic compounds

Versatility

Wide range of applications in various industries

Check Digit Verification of cas no

The CAS Registry Mumber 80683-81-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,8 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80683-81:
(7*8)+(6*0)+(5*6)+(4*8)+(3*3)+(2*8)+(1*1)=144
144 % 10 = 4
So 80683-81-4 is a valid CAS Registry Number.

80683-81-4SDS

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 11-methylsulfanylundecanoic acid

1.2 Other means of identification

Product number -
Other names 11-Methylmercapto-undecylsaeure

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:80683-81-4 SDS

80683-81-4Relevant articles and documents

A Mild Heteroatom (O -, N -, and S -) Methylation Protocol Using Trimethyl Phosphate (TMP)-Ca(OH) 2Combination

Tang, Yu,Yu, Biao

, (2022/03/27)

A mild heteroatom methylation protocol using trimethyl phosphate (TMP)-Ca(OH)2combination has been developed, which proceeds in DMF, or water, or under neat conditions, at 80 °C or at room temperature. A series of O-, N-, and S-nucleophiles, including phenols, sulfonamides, N-heterocycles, such as 9H-carbazole, indole derivatives, and 1,8-naphthalimide, and aryl/alkyl thiols, are suitable substrates for this protocol. The high efficiency, operational simplicity, scalability, cost-efficiency, and environmentally friendly nature of this protocol make it an attractive alternative to the conventional base-promoted heteroatom methylation procedures.

SYNTHESIS OF RACEMIC ALKALOID DIPTHALINE AND ITS STRUCTURAL ANALOGS AND THEIR ANTIHYPOXIC ACTIVITY

Biktimirova, L. A.,Likhovskikh, V. V.,Tolstikova, O. V.,Tolstikova, T. G.,Tolstikov, A. G.

, p. 843 - 846 (2007/10/02)

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