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14202-62-1

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14202-62-1 Usage

General Description

2,2-DIETHYL-1-PENTANOL is a chemical compound with the molecular formula C9H20O. It is an organic compound classified as a pentanol, which consists of a pentane chain with a hydroxyl group attached to one of the carbon atoms. 2,2-DIETHYL-1-PENTANOL is a clear, colorless liquid with a slightly fruity odor. It is commonly used as a solvent in various industrial applications, as well as a chemical intermediate in the production of pharmaceuticals, pesticides, and other organic compounds. It is also known for its use as a fragrance ingredient in perfumes and cosmetics. 2,2-DIETHYL-1-PENTANOL is relatively stable and has low toxicity, making it a versatile and widely used chemical in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 14202-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,0 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14202-62:
(7*1)+(6*4)+(5*2)+(4*0)+(3*2)+(2*6)+(1*2)=61
61 % 10 = 1
So 14202-62-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O/c1-4-7-9(5-2,6-3)8-10/h10H,4-8H2,1-3H3

14202-62-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-diethylpentan-1-ol

1.2 Other means of identification

Product number -
Other names 2,2-diethyl-1-penthanol

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:14202-62-1 SDS

14202-62-1Downstream Products

14202-62-1Relevant articles and documents

Lithium aluminum hydride-aluminum hydride reduction of sultones

Smith, Michael B.,Wolinsky, Joseph

, p. 101 - 106 (2007/10/02)

Lithium aluminum hydride-aluminum hydride reduction of secondary and tertiary (C-O) substituted γ-sultones or α-alkyl-β'-hydroxy γ-sultones yields mercapto alcohols and mercapto diols, respectively, in fair to good yield.These products result from S-O cleavage of the sultone ring.Primary sultones and α-dialkyl-β'-hydroxy γ-sultones give predominantly C-O cleavage to form sulfonic acid derivatives. β-Sultones are much less reactive toward the mixed hydride, and refluxing in dioxane is required for their reduction.

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