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10445-92-8

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10445-92-8 Usage

General Description

Pyridine, 2-(1-chloroethyl)- (7CI,8CI,9CI) is a specific type of chemical compound which is widely used in various laboratory and industrial applications. It is from the Pyridine family, a group of organic compounds whose base structure is a six-atom ring, with five carbon molecules and one nitrogen molecule. The orientation and position of the molecular substituents, namely the chloroethyl group in the 2-position, gives it its unique name and properties. Being a fairly complex structure, special attention is required for its handling and storage in accordance with strict safety guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 10445-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,4 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10445-92:
(7*1)+(6*0)+(5*4)+(4*4)+(3*5)+(2*9)+(1*2)=78
78 % 10 = 8
So 10445-92-8 is a valid CAS Registry Number.

10445-92-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-Chloroethyl)pyridine

1.2 Other means of identification

Product number -
Other names 2,6-DICARBOXYANILINE

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:10445-92-8 SDS

10445-92-8Downstream Products

10445-92-8Relevant articles and documents

Orientation towards asymmetric transfer hydrogenation of ketones catalyzed by (pyrazolyl)ethyl)pyridine Fe(II) and Ni(II) complexes

Magubane, Makhosazane N.,Alam, Mohd Gulfam,Ojwach, Stephen O.,Munro, Orde Q.

, p. 197 - 201 (2017)

Compounds 2-[1-(3,5-dimethylpyrazol-1-yl)ethyl]pyridine (L1) and 2-[1-(3,5-diphenylpyrazol-1-yl)ethyl]pyridine (L2) were obtained in a three-step procedure which involved the reduction of acetylpyridine using NaBH4, chlorination of the alcohol intermediate using SOCl2 and subsequent reaction with appropriate pyrazoles. Reactions of L1 and L2 with Ni(II) and Fe(II) halides produced the respective complexes Ni(L1)Br2 (1), Ni(L1)Cl2 (2), Fe(L1)Cl2 (3) and Ni(L2)Br2 (4) as racemic mixtures in moderate yields. The molecular structures of complexes 1 and 4 are dinuclear and mononuclear respectively. All the complexes (1–4) formed active catalysts for the transfer hydrogenation of ketones (THK) in 2-propanol at 82?°C affording conversions of 58%–84% within 48?h. The influence of catalyst structure, reaction conditions and identity of ketone substrates in the TH reactions have been successfully established.

SUBSTITUTED PYRAZOLES AND USES THEREOF

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Paragraph 0249; 0250, (2015/07/02)

The present invention provides for compounds of formula 0 and various embodiments thereof, and compositions comprising compounds of formula 0 and various embodiments thereof. In compounds of formula 0, the groups R1A, R1B, R1C, R1D, R2, R3, R4, R5 and R6 have the meaning as described herein. The present invention also provides for methods of using compounds of formula 0 and compositions comprising compounds of formula 0 as DLK inhibitors and for treating neurodegeneration diseases and disorders.

Lithiation of 2-chloromethylpyridine: Synthesis of 2-oxiranyl pyridines

Florio,Troisi

, p. 3175 - 3178 (2007/10/02)

Deprotonation of 2-chloromethylpyridine 1a with lithium diisopropylamide (LDA) in tetrahydrofuran (THF) at -78°C gives a red solution of 2-pyridiylchloromethyllithium 1b, which reacts with carbonyl compounds furnishing oxiranes 2.

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