Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1516-01-4

Post Buying Request

1516-01-4 Suppliers

Recommended suppliersmore

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

1516-01-4 Usage

General Description

2,4-Hexadienenitrile, also known as acrylonitrile, is a colorless, flammable liquid with a pungent, irritating odor. It is widely used in the production of acrylic fibers, resins, and plastics, as well as in the manufacturing of synthetic rubbers and adhesives. 2,4-Hexadienenitrile is also a key ingredient in the production of acrylamide, which is used to make polyacrylamide, a widely used flocculant in waste water treatment. However, 2,4-Hexadienenitrile is highly toxic and exposure to it can cause irritation to the skin, eyes, and respiratory system. It is also considered a potential carcinogen, and should be handled with caution in occupational and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 1516-01-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1516-01:
(6*1)+(5*5)+(4*1)+(3*6)+(2*0)+(1*1)=54
54 % 10 = 4
So 1516-01-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N/c1-2-3-4-5-6-7/h2-5H,1H3/b3-2+,5-4+

1516-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E,4E)-hexa-2,4-dienenitrile

1.2 Other means of identification

Product number -
Other names 2,4-Hexadienenitrile

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:1516-01-4 SDS

1516-01-4Relevant articles and documents

A new efficient method for the conversion of aldehydes into nitriles using ammonia and hydrogen peroxide

Erman,Snow,Williams

, p. 6749 - 6752 (2007/10/03)

Aldehydes were converted into the corresponding nitriles by a homogeneous reaction with ammonia and aqueous hydrogen peroxide in the presence of copper salts or complexes under mild conditions. (C) 2000 Elsevier Science Ltd.

Improved Synthesis of 3-Methylcholanthrene

Tang, Ping Wah,Maggiulli, Cataldo A.

, p. 3429 - 3432 (2007/10/02)

An improved synthesis of 7-methylindan-4-yl 1-naphthyl ketone (3), an important precursor of 3-methylcholanthrene (1), has been developed.The key intermediates for 3, 4-cyano-7-methylindan (2a) and 4-(ethoxycarbonyl)-7-methylindan (2b), were conveniently prepared in high yields by reaction of 1-(1-pyrrolidino)cyclopentene (6) with sorbonitrile (5a) or ethyl sorbate (5b), followed by aromatization with sulfur. 1-Naphthylmagnesium bromide (4b) in the presence of cuprous iodide reacted cleanly with 4-(chloromethanoyl)-7-methylindan (12) to give 3.The Friedel-Crafts acylation of naphthalene with 12 afforded 84percent of 3 and 16percent of β isomer 13.Alternatively, 3 was prepared in 75percent yield by condensation of Grignard reagent 4b with 2a in THF.Thermal annelation of 3 afforded 1 in 41.5percent yield.

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 1516-01-4