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50816-19-8

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50816-19-8 Usage

Chemical Properties

Clear colorless to yellow liquid

Uses

It is used to produce 8-phenylselanyl-octan-1-ol by reaction with diphenyl-diselane. The reaction occurs with reagent sodium borohydride and solvent ethanol at ambient temperature. The yield is about 96%. 8-Bromo-1-octanol was used in the synthesis of (E)-10-hydroxy-2-decenoic acid (royal jelly acid)1. It was also used in the synthesis of (Z)-14-methyl-9-pentadecenoic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 50816-19-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,1 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50816-19:
(7*5)+(6*0)+(5*8)+(4*1)+(3*6)+(2*1)+(1*9)=108
108 % 10 = 8
So 50816-19-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H17BrO/c9-7-5-3-1-2-4-6-8-10/h10H,1-8H2

50816-19-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Alfa Aesar

  • (H27628)  8-Bromo-1-octanol, 95%   

  • 50816-19-8

  • 1g

  • 526.0CNY

  • Detail
  • Alfa Aesar

  • (H27628)  8-Bromo-1-octanol, 95%   

  • 50816-19-8

  • 5g

  • 1932.0CNY

  • Detail
  • Alfa Aesar

  • (H27628)  8-Bromo-1-octanol, 95%   

  • 50816-19-8

  • 25g

  • 5937.0CNY

  • Detail
  • Aldrich

  • (294144)  8-Bromo-1-octanol  95%

  • 50816-19-8

  • 294144-1G

  • 411.84CNY

  • Detail
  • Aldrich

  • (294144)  8-Bromo-1-octanol  95%

  • 50816-19-8

  • 294144-5G

  • 1,623.96CNY

  • Detail

50816-19-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-Bromo-1-octanol

1.2 Other means of identification

Product number -
Other names 8-bromooctan-1-ol

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:50816-19-8 SDS

50816-19-8Relevant articles and documents

Influence of liquid crystalline formation on the phase behavior of side-chain liquid crystalline block copolymers

Ji, Liangliang,Chen, Xiaofang,Wu, Yanhong,Yang, Xiaoming,Tu, Yingfeng

, p. 147 - 154 (2015)

A series of narrowly distributed diblock copolymers composed of amorphous components and side-chain liquid crystalline (LC) polymer, poly (butyl acrylate)-block-poly [8-(4-cyano-4′-biphenyl)-1-octanoyl acrylate] (PBA-b-PCBOA), with side-chain LC block weight fraction (fw,PCBOA) ranging from 25% to 87%, were synthesized by atom transfer radical polymerization (ATRP). Their thermal property, LC behavior, bulk phase behavior and thin film morphology were studied by differential scanning calorimetry (DSC), polarizing optical microscope (POM), small-angle X-ray scattering (SAXS) techniques and atomic force microscopy (AFM), respectively. The results show the diblock copolymers with different composition could present sphere, lamellar and cylinder morphologies before the order-disorder transition. As the mesogen units self-organize to form smectic phase, the lamellar morphology dominates during the majority LC block weight fraction range (fw,PCBOA = 46%-77%) to minimized the surface energy. Interestingly, for spin-coated thin film, the lamella phase separation size decreased with increasing annealing time. For the copolymer with fw,PCBOA of 67%, a thermoreversible order-order transition (OOT) and lamella to lamella/modified layer (L/ML), were observed.

Identification and synthesis of the male produced volatiles of the carrion beetle, Oxelytrum erythrurum (Coleoptera: Silphidae)

Fockink, Douglas H.,Martins, Camila B.C.,Zarbin, Paulo H.G.

, p. 5353 - 5356 (2015)

Necrophagous beetles belonging to the family Silphidae are recognized as potentially useful in forensic investigations (to estimate post mortem interval). Gas chromatography analyses of extracts of aerations of adult Oxelytrum erythrurum revealed the presence of two male-specific compounds. These compounds were identified as (Z)-1,10-nonadecadiene (major) and 1-nonadecene (minor) using microderivatizations of the natural male extract, such as hydrogenation, partial reduction and methylthiolation, mass spectrum comparisons, and co-injections with authentic standards. Both compounds might be components of a pheromone responsible for sexual communication in this species.

Nucleophilic substitution reactions of unbranched alkyl amines using triazine reagents

Kitamura, Masanori,Kitaoka, Yuki,Fujita, Hikaru,Kunishima, Munetaka

supporting information, (2022/03/02)

Since amines are present in many organic, biological, and drug molecules, a strategy of synthesizing desired compounds by nucleophilic substitution reactions of these amines is very attractive. By using triazine reagents, we have found that nucleophilic substitution reactions of unbranched alkyl amines via morpholine derivatives are feasible. This method can be performed under milder reaction conditions than those in previously reported methods.

Synthesis method of (Z/E)-8-dodecen-1-alcohol acetate compound

-

Paragraph 0060; 0061; 0062; 0069-0071; 0078-0080, (2019/05/21)

The invention provides a synthesis method of a (Z/E)-8-dodecane-1-alcohol acetate compound. Specifically, the method includes the following steps: preparing 8-bromooctanol from 1,8-octanediol, then performing esterification reaction to obtain 8-Bromooctanol acetate, and then preparing omega-acetoxyoctanyl triphenyl phosphine bromide salt, and finally performing reaction through Scholoer-wittig toobtain (Z/E)-8-dodecene-1-alcohol acetate. The synthesis method has the advantages of high availability of raw materials, high yield and good selectivity, and is suitable for industrial production.

COMPOSITIONS AND METHODS FOR DELIVERY OF MACROMOLECULES

-

Paragraph 00432; 00437; 00438, (2019/06/23)

The present disclosure provides endosomal disruptors, which are useful for facilitating delivery of a macromolecule to the cytoplasm of a cell. The present disclosure provides compositions comprising an endosomal disruptor and a macromolecule. The present disclosure provides methods of delivering a macromolecule to the cytoplasm of a cell.

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