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4676-74-8

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4676-74-8 Usage

Chemical structure

1,5-epoxyrefers to a group of chemicals that contain an epoxy or oxirane ring structure with a five-carbon chain.

Industrial applications

These chemicals are commonly used in industrial applications, such as adhesives, coatings, and composites, due to their ability to crosslink and form strong, durable bonds.

Intermediates

1,5-epoxycompounds are also used as intermediates in the production of plastics, resins, and other synthetic materials.

Potential hazards

They are known to be potentially hazardous to human health and the environment, and exposure to these chemicals should be limited and carefully controlled.

Ongoing research and regulation

Research and regulation of 1,5-epoxychemicals are ongoing to ensure their safe use and minimize the associated risks.

Check Digit Verification of cas no

The CAS Registry Mumber 4676-74-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,7 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4676-74:
(6*4)+(5*6)+(4*7)+(3*6)+(2*7)+(1*4)=118
118 % 10 = 8
So 4676-74-8 is a valid CAS Registry Number.

4676-74-8SDS

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-butyltetrahydropyran

1.2 Other means of identification

Product number -
Other names 2-n-butyloxane

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:4676-74-8 SDS

4676-74-8Downstream Products

4676-74-8Relevant articles and documents

Piperidine and azetidine formation by direct cyclization of diols with N-nonsubstituted sulfonamide under the Mitsunobu conditions utilizing (cyanomethylene)tributylphosphorane (CMBP) and its application to the synthesis of lupinine

Hamaguchi, Takumi,Hishida, Hideyuki,Horikawa, Mitsuyo,Inai, Makoto,Kaku, Hiroto,Kitamura, Kei,Kubo, Akiko,Sonoda, Yuhei,Taniguchi, Yuri,Tsunoda, Tetsuto

, p. 1525 - 1535 (2020/01/28)

(Cyanomethylene)tributylphosphorane (CMBP) can promote the Mitsunobu reaction of 1,3- and 1,5-diols with N-nonsubstituted sulfonamides, such as tosylamide (TsNH2) and 3,3-dimethoxypropylsulfonamide (DimpsNH2), to prepare azetidine and piperidine ring systems directly. Utilizing this methodology, lupinine, a biologically active piperidine alkaloid, was synthesized.

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