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CAS

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135312-82-2

2-Bromotetradecanoic acid is a brominated long-chain saturated fatty acid with the chemical formula C14H27BrO2. It features a carbon chain with a bromine atom attached, providing unique properties that make it useful in various chemical reactions and processes.

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  • 135312-82-2 Structure

  • Basic information

    1. Product Name: 2-BROMOTETRADECANOIC ACID
    2. Synonyms: 2-BROMOTETRADECANOIC ACID;2-BROMOMYRISTIC ACID;ALPHA-BROMOMYRISTIC ACID;A-BROMOMYRISTIC ACID
    3. CAS NO:135312-82-2
    4. Molecular Formula: C14H27BrO2
    5. Molecular Weight: 307.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135312-82-2.mol

  • Chemical Properties

    1. Melting Point: 41-43°C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. BRN: 1781090
    10. CAS DataBase Reference: 2-BROMOTETRADECANOIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-BROMOTETRADECANOIC ACID(135312-82-2)
    12. EPA Substance Registry System: 2-BROMOTETRADECANOIC ACID(135312-82-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 135312-82-2(Hazardous Substances Data)

135312-82-2 Usage

Uses

Used in Pharmaceutical Industry:
2-Bromotetradecanoic acid is used as a building block for the synthesis of various organic compounds, particularly in the development of pharmaceuticals. Its unique structure with a bromine atom allows for versatile chemical modifications, contributing to the creation of new drug candidates.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Bromotetradecanoic acid serves as a precursor for the synthesis of compounds with potential applications in crop protection and pest control. Its bromine-containing structure can be utilized to develop novel agrochemicals with improved efficacy and selectivity.
It is important to handle 2-Bromotetradecanoic acid with care, as brominated compounds can pose hazards if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 135312-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,3,1 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 135312-82:
(8*1)+(7*3)+(6*5)+(5*3)+(4*1)+(3*2)+(2*8)+(1*2)=102
102 % 10 = 2
So 135312-82-2 is a valid CAS Registry Number.

135312-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-BROMOTETRADECANOIC ACID

1.2 Other means of identification

Product number -
Other names 2-Bromotetradecanoic 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:135312-82-2 SDS

135312-82-2Upstream product

135312-82-2Relevant articles and documents

Mesoionic 5-alkyl-1,3-dithiolium-4-thiolates: Synthesis and brine shrimp toxicity

De Almeida, Paulo Afonso,Da Silva, Tania Maria Sarmento,Echevarria, Aurea

, p. 593 - 600 (2007/10/03)

A series of twelve 1,3-dithiolium-4-thiolate mesoionic compounds were synthesized and characterized. The synthetical approach starting from α-bromoalkanoic acids to obtain the corresponding 2-N-morpholino-dithiocarbamoyl-carboxylic acids that by on-pot reaction with carbon disulfide and acetic anhydride in triethylamine formed not isolate intermediates, 1,3-dithiolium-4-olates. After, the 2-N-morpholino-5-alkyl-1,3-dithiolium-4-thiolates were obtained by retro 1,3-dipolar addition reactions. The alkyl moiety linked to C-5 of heterocyclic ring permitted the increase of the hydrophobic character and this effect was evaluated on Artemia salina lethality. The results indicated a bell-shaped relationship between the number of carbon of side chain in mesoionic derivatives and LD50 in brine shrimp toxicity assays.

Syntheses of 2-(2-Hydroxyethylamino) Fatty Acids

Xianxian, Du

, p. 123 - 124 (2007/10/02)

Eight 2-(2-hydroxyethylamino) fatty acids, 2-(2-hydroxyethylamino)decanoic, -undecanoic, -dodecanoic, -tetradecanoic, -hexadecanoic, -octadecanoic, -nonadecanoic, and docosanoic acid, were synthesized by reacting 2-bromo fatty acids with more than 3 mol of 2-aminoethanol.The surface tension and the critical micelle concentration were determined for these compounds.

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