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1-Hexanol, 6-chloro-, 4-methylbenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 71042-21-2 Structure
  • Basic information

    1. Product Name: 1-Hexanol, 6-chloro-, 4-methylbenzenesulfonate
    2. Synonyms:
    3. CAS NO:71042-21-2
    4. Molecular Formula: C13H19ClO3S
    5. Molecular Weight: 290.811
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 71042-21-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-Hexanol, 6-chloro-, 4-methylbenzenesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Hexanol, 6-chloro-, 4-methylbenzenesulfonate(71042-21-2)
    11. EPA Substance Registry System: 1-Hexanol, 6-chloro-, 4-methylbenzenesulfonate(71042-21-2)
  • 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: 71042-21-2(Hazardous Substances Data)

71042-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71042-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,4 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71042-21:
(7*7)+(6*1)+(5*0)+(4*4)+(3*2)+(2*2)+(1*1)=82
82 % 10 = 2
So 71042-21-2 is a valid CAS Registry Number.

71042-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chlorohexan-1-ol,4-methylbenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names toluene-4-sulfonic acid 6-chlorohexyl ester

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:71042-21-2 SDS

71042-21-2Relevant articles and documents

BODIPY protein misfolding probe Hal-BODIPY, preparation method and application thereof

-

Paragraph 0041-0043; 0046; 0047, (2021/01/29)

The invention discloses a BODIPY protein misfolding probe Halo-BODIPY, a preparation method and application thereof, wherein the structural formula of the fluorescent probe is shown as a formula I inthe specification. According to the invention, the micro

FLUORESCENCE DYE

-

Page/Page column 28; 29, (2020/07/07)

The present invention relates to compound according to formulas (1), (15), (16) or (17), the use of the compounds as a fluorescent dye, and a fluorescent dye comprising the compounds. The invention also relates to a method for fluorescence-based identific

Preparation method of 1-chloro-6-iodohexane

-

Paragraph 0011; 0013, (2019/04/09)

The invention discloses a preparation method of 1-chloro-6-iodohexane. The preparation method comprises the steps of with 6-chloro-1-hexanol and p-toluene sulfochloride as the materials and benzene ortoluene as a solvent, reacting at (-5)-(5) DEG C for 2-5 hours under the effects of a phase transfer catalyst and an acid-binding agent so as to prepare 4-methylbenzenesulfonic acid-6-chlorohexyl ester, and carrying out reflux reaction on 4-methylbenzenesulfonic acid-6-chlorohexyl ester and sodium iodide for 0.5-3 hours, so as to prepare 1-chloro-6-iodohexane. The preparation method has the characteristics of easiness in operation, simplicity and convenience in after-treatment and relatively high yield.

DYES FOR ANALYSIS OF SOLUBLE PROTEIN AGGREGATES OR MISFOLDED PROTEIN OLIGOMERS

-

Paragraph 0099; 00100, (2019/10/01)

Dye and compositions to monitor the multistep protein aggregation process in both test tubes and live cells are provided. These dyes can detect misfolded protein oligomers and distinguish insoluble protein aggregates from misfolded oligomers. Applications of these dyes include measuring kinetics of protein aggregation, monitoring aggregation of specific proteins in intact live cells, monitoring aggregation of cellular proteome in intact live cells, and tracking the time course of protein aggregation in cells under stress conditions.

An acid/alkali double stimulus responsive nano container and its preparation method

-

Paragraph 0039-0041; 0057; 0073, (2018/11/22)

The invention discloses an acid/base double stimulation responsive nanometer container and a preparation method thereof. According to the nanometer container, mesoporous nanometer silicon dioxide is adopted as a framework; a host-guest compound is formed based on host pillar[5]arene and a guest molecular chain 1,6-(1-(1-methyl)imida zolehexyl)hexamethylene diamine; a supramolecular valve is formed on the surface of a microsphere through modification; a metal corrosion inhibitor is loaded in the microsphere; under the action of pH stimulation, macrocyclic pillar[5]arene in the nanometer container can move, thereby achieving controllable release of the metal corrosion inhibitor; and after the metal corrosion inhibitor enters a coating, metal corrosion can be effectively inhibited. The nanometer container disclosed by the invention has the advantages that the function of response to various external stimuluses can be achieved; double response to acid/base stimulation can be achieved; and the prospect of application to the fields of drug delivery, intelligent anti-corrosive coating and the like is broad.

Copper-catalyzed cross-coupling reaction of organoboron compounds with primary alkyl halides and pseudohalides

Yang, Chu-Ting,Zhang, Zhen-Qi,Liu, Yu-Chen,Liu, Lei

supporting information; experimental part, p. 3904 - 3907 (2011/05/15)

Non-activated alkyl electrophiles, including alkyl iodides, bromides, tosylates, mesylates, and even chlorides, underwent copper-catalyzed cross-coupling with aryl boron compounds and alkyl 9-BBN reagents (see scheme; 9-BBN=9-borabicyclo[3.3.1]nonane). The reactions proceed with practically useful reactivities and thus complement palladium- and nickel-catalyzed Suzuki-Miyaura coupling reactions of alkyl halides.

Pheromone synthesis. Part 244: Synthesis of the racemate and enantiomers of (11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male Drosophila melanogaster to show its (S)-isomer and racemate as bioactive

Mori, Kenji,Shikichi, Yasumasa,Shankar, Shruti,Yew, Joanne Y.

experimental part, p. 7161 - 7168 (2010/10/01)

The enantiomers of (11Z,19Z)-3-acetoxy-11,19-octacosadien-1-ol were synthesized from the enantiomers of 3,4-epoxy-1-butanol PMB ether. Its racemate was also synthesized. Its (S)-isomer and racemate were shown to possess the same pheromone activity as CH503, a long-lived inhibitor of male courtship in Drosophila melanogaster, although the racemate was less active.

Approaches towards the synthesis of fluoro(cyclo)alkylamines

Windhorst,Bechger,Visser,Menge,Leurs,Timmerman,Herscheid

, p. 35 - 40 (2007/10/03)

The synthesis of fluoro(cyclo)alkylamines 1-amino-6-fluorohexane (1), 1-amino-7-fluoroheptane (2), cis/trans-4-fluorocyclohexylamine (3a,b) and cis-4-fluoromethylcyclohexylamine (4) has been investigated for use as synthons for histamine receptor ligands for use in PET.

Convenient synthesis of large tetraazamacrocycles bearing alkylene, cyclophane and crown ether type skeletons

Tomohiro,Ahmadi Avval,Okuno

, p. 639 - 640 (2007/10/02)

A series of large tetraazamacrocycles with 28- to 44-membered rings consisting of alkylene, phenylene or ether type backbones has been prepared without the use of high-dilution conditions in practically significant yields (25-42%). The reaction can be car

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