123005-17-4

• 

• Basic information

  1. Product Name: Quinoline, 2,4-dicyclohexyl-
  2. Synonyms:
  3. CAS NO:123005-17-4
  4. Molecular Formula: C21H27N
  5. Molecular Weight: 293.452
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 123005-17-4.mol
  9. Article Data: 21

• 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: Quinoline, 2,4-dicyclohexyl-(CAS DataBase Reference)
  10. NIST Chemistry Reference: Quinoline, 2,4-dicyclohexyl-(123005-17-4)
  11. EPA Substance Registry System: Quinoline, 2,4-dicyclohexyl-(123005-17-4)

• 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: 123005-17-4(Hazardous Substances Data)

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• Upstream product
• Downstream Products
• Article

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123005-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123005-17-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,0,0 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 123005-17:
(8*1)+(7*2)+(6*3)+(5*0)+(4*0)+(3*5)+(2*1)+(1*7)=64
64 % 10 = 4
So 123005-17-4 is a valid CAS Registry Number.

123005-17-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name	2,4-dicyclohexylquinoline

1.2 Other means of identification

Product number	-
Other names	Quinoline,2,4-dicyclohexyl

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:123005-17-4 SDS

123005-17-4Upstream product

• 91-22-5 quinoline 
• 110-82-7 cyclohexane 
• 125764-09-2 tetraethylammonium bis<α,α-bis(trifluoromethyl)benzenemethanolato(2-)-C²,O>cyclohexylsilicate 
• 108-85-0 1-bromocyclohexane 
• 70091-69-9 3,3,3',3'-tetrakis(trifluoromethyl)-1,1'(3H,3'H)-spirobi<2,1-benzoxasilole> 
• 4441-56-9 cyclohexylboronic acid 
• 126812-30-4 1,3-dioxoisoindolin-2-yl cyclohexanecarboxylate 
• 98-89-5 Cyclohexanecarboxylic acid 
• 41320-40-5 <<(methylthio)thiocarbonyl>oxy>cyclohexane 
• 626-62-0 Cyclohexyl iodide 
• 703-61-7 2,4-dichloroquinoline 
• 110-83-8 cyclohexene 

123005-17-4Downstream Products

123005-17-4Relevant articles and documents

A Fe(III)/NaBH4-Promoted Free-Radical Hydroheteroarylation of Alkenes

Liang, Bingyu,Wang, Qinglong,Liu, Zhong-Quan

, p. 6463 - 6465 (2017)

A free-radical-mediated intermolecular hydroheteroarylation of simple alkenes was developed. Through simply mixing heteroarenes, alkenes, Fe(III), and NaBH4 at 0 °C together, a wide range of alkylated heteroarenes could be afforded in moderate to excellent yields within 1 h.

Time-Resolved EPR Revealed the Formation, Structure, and Reactivity of N -Centered Radicals in an Electrochemical C(sp3)-H Arylation Reaction

Alhumade, Hesham,Gao, Renfei,Huang, Cunlong,Lei, Aiwen,Liu, Yichang,Liu, Zhao,Qi, Xiaotian,Shi, Biyin,Wang, Shengchun

supporting information, p. 20863 - 20872 (2021/12/14)

Electrochemical synthesis has been rapidly developed over the past few years, while a vast majority of the reactions proceed through a radical pathway. Understanding the properties of radical intermediates is crucial in the mechanistic study of electroche

Visible-light-mediated photoredox minisci C-H alkylation with alkyl boronic acids using molecular oxygen as an oxidant

Dong, Jianyang,Yue, Fuyang,Song, Hongjian,Liu, Yuxiu,Wang, Qingmin

supporting information, p. 12652 - 12655 (2020/11/02)

Herein, we report a protocol for direct visible-light-mediated Minisci C-H alkylation reactions of heteroarenes with alkyl boronic acids using molecular oxygen as the sole oxidant. This mild protocol uses an inexpensive, green oxidant; permits efficient functionalization of various N-heteroarenes with a broad range of primary and secondary alkyl boronic acids; and is scalable to the gram level. We demonstrated the practicality and sustainability of the protocol by preparing or functionalizing several pharmaceuticals and natural products.

Cross-Dehydrogenative Coupling of Strong C(sp3)-H with N-Heteroarenes through Visible-Light-Induced Energy Transfer

An, Guanghui,Li, Guangming,Tian, Chao,Tian, Haitao,Yang, Hui

supporting information, p. 7709 - 7715 (2020/10/09)

The sustainable cross-dehydrogenative coupling of strong C(sp3)-H with N-heteroarenes has been developed using an efficient organic photocatalyst. It features atomic- and step-economy, and acid-free conditions. Mechanism studies suggest a previous elusive

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