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71655-36-2

Dodecanoic acid, 12-hydroxy-, Methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 71655-36-2 Structure

  • Basic information

    1. Product Name: Dodecanoic acid, 12-hydroxy-, Methyl ester
    2. Synonyms: Dodecanoic acid, 12-hydroxy-, Methyl ester
    3. CAS NO:71655-36-2
    4. Molecular Formula: C13H26O3
    5. Molecular Weight: 230.34374
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 71655-36-2.mol

  • Chemical Properties

    1. Melting Point: 33.2-34.5 °C
    2. Boiling Point: 311.3±15.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.943±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 15.20±0.10(Predicted)
    10. CAS DataBase Reference: Dodecanoic acid, 12-hydroxy-, Methyl ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: Dodecanoic acid, 12-hydroxy-, Methyl ester(71655-36-2)
    12. EPA Substance Registry System: Dodecanoic acid, 12-hydroxy-, Methyl ester(71655-36-2)

  • 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: 71655-36-2(Hazardous Substances Data)

71655-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71655-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,5 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71655-36:
(7*7)+(6*1)+(5*6)+(4*5)+(3*5)+(2*3)+(1*6)=132
132 % 10 = 2
So 71655-36-2 is a valid CAS Registry Number.

71655-36-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 12-hydroxydodecanoate

1.2 Other means of identification

Product number -
Other names methyl ester of 12-hydroxydodecanoic acid

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:71655-36-2 SDS

71655-36-2Relevant articles and documents

PROCESS FOR PRODUCING DODECANE-1, 12-DIOL BY REDUCTION OF LAURYL LACTONE PRODUCED FROM THE OXIDATION OF CYCLODODECANONE

-

Paragraph 00130, (2013/08/15)

A process for synthesizing dodecane-1,12-diol, and by-products thereof, by the reduction of lauryl lactone produced from the oxidation of cyclododecanone.

Direct terminal alkylamino-functionalization via multistep biocatalysis in one recombinant whole-cell catalyst

Schrewe, Manfred,Ladkau, Nadine,Buehler, Bruno,Schmid, Andreas

supporting information, p. 1693 - 1697 (2013/07/19)

Direct and regiospecific amino-functionalization of non-activated carbon could be achieved using one recombinant microbial catalyst. The presented proof of concept shows that heterologous pathway engineering allowed the construction of a whole-cell biocatalyst catalyzing the terminal amino-functionalization of fatty acid methyl esters (e.g., dodecanoic acid methyl ester) and alkanes (e.g., octane). By coupling oxygenase and transaminase catalysis in vivo, both substrates are converted with absolute regiospecificity to the terminal amine via two sequential oxidation reactions followed by an amination step. Such demanding chemical three-step reactions achieved with a single catalyst demonstrate the tremendous potential of whole-cell biocatalysts for the production of industrially relevant building blocks. Copyright

Iridium-catalyzed oxidative methyl esterification of primary alcohols and diols with methanol

Yamamoto, Nobuyuki,Obora, Yasushi,Ishii, Yasutaka

experimental part, p. 2937 - 2941 (2011/05/30)

Oxidative methyl esterification of primary alcohols and diols with methanol was successfully achieved, using acetone as a hydrogen acceptor, under the influence of an iridium complex combined with 2-(methylamino)ethanol (MAE) as catalyst.

Highly efficient deacetylation by use of the neutral organotin catalyst [tBu2SnOH(Cl)]2

Orita, Akihiro,Hamada, Yuuki,Nakano, Takehiko,Toyoshima, Shinji,Otera, Junzo

, p. 3321 - 3327 (2007/10/03)

Deprotection of acetyl esters is effected cleanly by the neutral organotin catalyst, [tBu2SnOH(Cl)]2. The mildness of the reaction gives rise to great synthetic versatility and in the process a variety of functional groups are tolerated. Differentiations between primary, secondary, and tertiary alcohols and between acetyl ester and other esters are feasible. No racemization occurs with chiral acetyl esters. Exclusive deprotection of primary acetyl esters in carbohydrates and nucleosides is observed. The crude product thus obtained can be used for further reactions without purification.

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