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4417-86-1

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4417-86-1 Usage

General Description

2,4-Dihydroxy-3,3-dimethylbutanamide is a chemical compound with the molecular formula C6H13NO3. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 2,4-DIHYDROXY-3,3-DIMETHYLBUTANAMIDE is a derivative of butyric acid and contains two hydroxyl groups and a dimethyl substitution on the carbon chain. It is a white crystalline solid at room temperature and is slightly soluble in water and organic solvents. 2,4-Dihydroxy-3,3-dimethylbutanamide is commonly used in research and industrial applications due to its unique chemical structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 4417-86-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,1 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4417-86:
(6*4)+(5*4)+(4*1)+(3*7)+(2*8)+(1*6)=91
91 % 10 = 1
So 4417-86-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO3/c1-6(2,3-8)4(9)5(7)10/h4,8-9H,3H2,1-2H3,(H2,7,10)/t4-/m0/s1

4417-86-1SDS

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 2,4-Dihydroxy-3,3-dimethylbutanamide

1.2 Other means of identification

Product number -
Other names (+-)-2,4-Dihydroxy-3,3-dimethyl-buttersaeure-amid

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:4417-86-1 SDS

4417-86-1Relevant articles and documents

Parke,Lawson

, p. 2869,2871 (1941)

One-pot synthesis of N-substituted pantolactams from pantolactone

Barrios, Ivana,Camps, Pelayo,Comes-Franchini, Mauro,Mu?oz-Torrero, Diego,Ricci, Alfredo,Sánchez, Laura

, p. 1971 - 1979 (2007/10/03)

Rac-N-substituted pantolactams (5) are readily obtained in medium to good yields by reaction of rac-pantolactone (1) with primary amines under acid catalysis, whether at 250°C in a pressure reactor or under microwave irradiation. It appears that the amine can react with pantolactone at the carbonyl carbon atom to give a hydroxyamide (3) in a reversible way and at the methylene carbon atom to give a γ-amino acid (4). The last one on dehydration would give the corresponding pantolactam (5).

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