Welcome to LookChem.com Sign In|Join Free

CAS

  • or

5326-81-8

Post Buying Request

5326-81-8 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5326-81-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5326-81-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5326-81:
(6*5)+(5*3)+(4*2)+(3*6)+(2*8)+(1*1)=88
88 % 10 = 8
So 5326-81-8 is a valid CAS Registry Number.

5326-81-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-N-hexylacetamide

1.2 Other means of identification

Product number -
Other names Acetamide, 2-chloro-N-hexyl-

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:5326-81-8 SDS

5326-81-8Relevant articles and documents

New interlocked molecules generated from a podand containing urea units and imidazolium salts using an anion template

Tomapatanaget, Boosayarat,Tuntulani, Thawatchai,Wisner, James A.,Beer, Paul D.

, p. 663 - 666 (2004)

A podand containing urea units (L) was found to form interlocked structures with 2,5-dihexylamide imidazolium salts (3·X), 2,5-dihexyl imidazolium salts (4·X), and 2,5-dihexyl benzoimidazolium salts (5·X), where X=Cl-, Br-, and PF6 - using anions as templates. The binding ability of L and guest molecules was evaluated by 1H NMR titrations in CDCl3. It was found that L could form complexes with guest molecules in the following order, 3·X>5·X>4·X. Stabilities of the complexes also depended on shape of the templated anions: Cl->Br -?PF6-. Hydrogen bonding and π-π stacking interactions played an important role in the self-assembling of these interlocked molecules.

2,5-dialkylacetamide-1,3,4-thiadiazole for biodegradable lubricating oil additives, and preparation method thereof

-

Paragraph 0041, (2017/06/02)

The invention discloses 2,5-dialkylacetamide-1,3,4-thiadiazole for biodegradable lubricating oil additives, and a preparation method thereof, wherein the structure of the 2,5-dialkylacetamide-1,3,4-thiadiazole is represented by a formula (1), R is a C1-C30 linear chain or branched chain alkyl group, 2,5-dimercapto-1,3,4-thiadiazole, n-butylamine, dodecylamine and chloroacetyl chloride are adopted as raw materials, triethylamine is adopted as an acid binding agent, dichloromethane is adopted as a solvent, an intermediate alkyl chloroacetamide is firstly obtained, and then the target product is obtained. According to the present invention, the source of the used raw materials is sufficient, the price of the used raw materials is low, the prepared intermediate chloroacetamide uses triethylamine as the acid binding agent, the synthesis process condition is mild, the process route is simple, the yield is high, and the obtained product has excellent extreme pressure wear resistance, has the good biodegradation performance after the use, and is the environmentally friendly multifunctional lubricating oil additive.

Alkyl acetamidobenzotriazole derivative lubricating oil additive and preparation method thereof

-

Paragraph 0045, (2018/04/01)

The invention discloses a biodegradable alkyl acetamidobenzotriazole derivative lubricating oil additive which does not contain sulfur, phosphorus, halogens and metal elements as well as a preparation method and application thereof. The preparation method comprises the following steps: under the action of alkali, performing amidation on alkyl amine and chloroacetyl chloride to obtain alkyl chloroacetamide; and then performing a nucleophilic substitution reaction with benzotriazole to obtain a target compound of a formula I. The preparation method disclosed by the invention is simple in preparation method, mild in process condition, easily available in raw material, low in preparation cost and high in synthetic yield. The novel alkyl acetamidobenzotriazole derivative can be independently used as an extreme pressure anti-wear corrosion-resistant additive of lubricating oil, also can be used with other lubricating oil additives in a compound manner, also can be used in common working conditions and high-temperature working conditions, can improve the bearing capacity of basic oil obviously and improve the anti-wear performance, and is the lubricating oil additive which is environmentally friendly and multi-functional. The formula I is as shown in the specification.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 5326-81-8