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1-Dodecene, 12-bromo-, also known as 1-Dodecene,12-broMo-, is a chemical compound with the molecular formula C12H23Br. It is an alkene, a type of hydrocarbon characterized by the presence of one or more carbon-carbon double bonds. 1-Dodecene,12-broMofeatures a bromo group, indicating that a bromine atom is attached to the 12th carbon atom in the molecular chain. This unique structure endows 1-Dodecene,12-broMowith versatile applications in various industries.

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  • 99828-63-4 Structure
  • Basic information

    1. Product Name: 1-Dodecene,12-broMo-
    2. Synonyms: 1-Dodecene,12-broMo-;12-Bromododec-1-ene
    3. CAS NO:99828-63-4
    4. Molecular Formula: C12H23Br
    5. Molecular Weight: 247.21502
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 99828-63-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 270.2±9.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.052±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-Dodecene,12-broMo-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Dodecene,12-broMo-(99828-63-4)
    11. EPA Substance Registry System: 1-Dodecene,12-broMo-(99828-63-4)
  • 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: 99828-63-4(Hazardous Substances Data)

99828-63-4 Usage

Uses

Used in Organic Synthesis:
1-Dodecene,12-broMois used as a building block in organic synthesis for the production of various other chemicals and polymers. Its unique structure allows for the creation of a wide range of compounds with different properties and applications.
Used in Surfactant Production:
In the chemical industry, 1-Dodecene,12-broMois used as a raw material in the production of surfactants. Surfactants are compounds that reduce the surface tension between liquids and solids, making them essential in various applications such as detergents, cleaners, and emulsifiers.
Used in Detergent Production:
1-Dodecene,12-broMois utilized in the manufacturing process of detergents, which are cleaning agents used in various household and industrial applications. 1-Dodecene,12-broMocontributes to the detergent's effectiveness in removing dirt and stains.
Used in Lubricant Production:
1-Dodecene,12-broMois also used in the production of lubricants, which are substances that reduce friction between moving parts in machinery. 1-Dodecene,12-broMohelps improve the performance and longevity of lubricants, ensuring smooth operation and reducing wear and tear.
Used in Pharmaceutical Synthesis:
1-Dodecene,12-broMoserves as an intermediate in the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to advancements in medicine and healthcare.
Used in Agrochemical Synthesis:
In the agrochemical industry, 1-Dodecene,12-broMois used as an intermediate in the synthesis of various agrochemicals, such as pesticides and herbicides. Its involvement in the production process helps create effective solutions for agricultural challenges and crop protection.

Check Digit Verification of cas no

The CAS Registry Mumber 99828-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,8,2 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 99828-63:
(7*9)+(6*9)+(5*8)+(4*2)+(3*8)+(2*6)+(1*3)=204
204 % 10 = 4
So 99828-63-4 is a valid CAS Registry Number.

99828-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 12-bromododec-1-ene

1.2 Other means of identification

Product number -
Other names 12-bromo-1-dodecene

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:99828-63-4 SDS

99828-63-4Relevant articles and documents

A facile asymmetric synthesis of (S)-14-methyl-1-octadecene, the sex pheromone of the peach leafminer moth

Zhang, Tao,Ma, Wei-Li,Li, Tian-Rui,Wu, Jia,Wang, Jun-Run,Du, Zhen-Ting

, p. 5201 - 5208 (2013/06/27)

An asymmetric synthesis of 14-methyl-1-octadecene, the sex pheromone of the peach leafminer moth has been achieved. The target molecule was synthesized in six linear steps and in 30.3% overall yield from commercially available hexanoyl chloride, (S)-4-benzyloxazolidin-2-one and 1,9-nonanediol. The hexanoyl chloride was connected with (S)-4-benzyloxazolidin-2-one, and with the induction of the chiral oxazolidinone auxiliary, after chiral methylation, LAH reduction and then tosylation gave the chiral key intermediate 5 in high stereoselectivity. 1,9-Nonanediol, was selectively brominated, THP protected and subjected to Li2CuCl4-mediated C-C coupling to afford a C12 intermediate. The target molecule, (S)-14-methyl-1-octadecene, was obtained after the two parts were subjected to a second Li 2CuCl4-mediated C-C coupling. Our synthetic approach represents the first time a substrate-control asymmetric synthesis of (S)-14-methyl-1-octadecene has been reported.

A photoirradiative phase-vanishing method: Efficient generation of HBr from alkanes and molecular bromine and its use for subsequent radical addition to terminal alkenes

Matsubara, Hiroshi,Tsukida, Masaaki,Ishihara, Daisuke,Kuniyoshi, Kenji,Ryu, Ilhyong

experimental part, p. 2014 - 2018 (2010/10/02)

A triphasic phase-vanishing (PV) system comprised of an alkane, perfluorohexanes, and bromine was successfully combined by photoirradiation to efficiently generate hydrogen bromide, which underwent radical addition with 1-alkenes in the hydrocarbon layer to afford terminal bromides in high yields. Georg Thieme Verlag Stuttgart.

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