What is the 2-METHYL-1,3-PROPANEDIOL?

2-METHYL-1,3-PROPANEDIOL is colourless liquid, while it's Molecular Formula is C4H10O2. colourless liquid β-Hydroxyisobutanol is used as a reagent in the synthesis of pyrazolo[1,5-a]pyridinecarbonyl-substituted spirocyclic piperidine ketals as inhibitors of HCV protein NS4B and of hepatitis C viral replication and their lack of cytotoxicity in human cells.

What is the CAS number for 2-METHYL-1,3-PROPANEDIOL?

The CAS number of 2-METHYL-1,3-PROPANEDIOL is 2163-42-0.

What is 2-METHYL-1,3-PROPANEDIOL (2163-42-0) used for?

2-METHYL-1,3-PROPANEDIOL, also known as β-Hydroxyisobutanol, is a chemical compound with the molecular formula C4H10O2. It is a diol, which means it contains two hydroxyl (-OH) groups. This organic compound is a colorless liquid with a slight odor and is soluble in water. It is commonly used as a building block in the synthesis of various pharmaceuticals and other chemical products.InChI:InChI=1/C4H10O2/c1-4(2-5)3-6/h4-6H,2-3H2,1H3

High Quality Chinese Factory supply 2163-42-0 2-METHYL-1,3-PROPANEDIOL

Molecular Formula:C4H10O2
Molecular Weight:90.1222
Appearance/Colour:colourless liquid
Vapor Pressure:0.0225mmHg at 25°C
Melting Point:-91 °C(lit.)
Refractive Index:n20/D 1.445(lit.)
Boiling Point:221.2 °C at 760 mmHg
PKA:14.51±0.10(Predicted)
Flash Point:102.5 °C
PSA：40.46000
Density:1.001 g/cm³
LogP:-0.39290

2-METHYL-1,3-PROPANEDIOL(Cas 2163-42-0) Usage

InChI:InChI=1/C4H10O2/c1-4(2-5)3-6/h4-6H,2-3H2,1H3

2163-42-0 Relevant articles

-

Bailey,W.J. et al.

, p. 1724 - 1725 (1963)

INDOLE DERIVATIVES AS ALPHA-1 -ANTITRYPSIN MODULATORS FOR TREATING ALPHA-1 -ANTITRYPSIN DEFICIENCY (AATD)

-

Paragraph 00234; 00316; 00778, (2021/10/11)

Indole derivatives as alpha-l-antitrypsi...

Method for preparing 2-methyl-1, 3-propylene glycol from isobutene

-

Paragraph 0054-0055; 0061; 0063; 0079; 0082-0083; 0086-0087;, (2021/02/10)

The invention discloses a method for pre...

Manganese(I)-Catalyzed β-Methylation of Alcohols Using Methanol as C1 Source

Kaithal, Akash,van Bonn, Pit,H?lscher, Markus,Leitner, Walter

supporting information, p. 215 - 220 (2019/12/03)

Highly selective β-methylation of alcoho...

Direct hydrocarbonylation process

-

Page/Page column 4-5, (2010/02/17)

A direct hydrocarbonylation process for ...

2163-42-0 Process route

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 75-07-0,9002-91-9
acetaldehyde

: 115-77-5
Pentaerythritol

: 2163-42-0
2-methyl-1.3-propanediol

: 4704-94-3
2-hydroxymethyl-1,3-propanediol

: 504-63-2
trimethyleneglycol

Conditions

Conditions	Yield
With sodium hydroxide; sulfuric acid; hydrogen; 5% activated charcoal-supported ruthenium catalyst; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; 1.) 25 deg C, 30 min, 2.) 50 psi, 25 deg C, 4 h;
With sodium hydroxide; sulfuric acid; hydrogen; Ru-carbon; Yield given. Multistep reaction. Yields of byproduct given; 1.) 25 deg C, 30 min, 2.) 50 psi, 25 deg C 4 h;

: 75-24-1
trimethylaluminum

: 556-52-5
oxiranyl-methanol

: 2163-42-0
2-methyl-1.3-propanediol

: 584-03-2
1,2-dihydroxybutane

Conditions

Conditions	Yield
trimethylaluminum; oxiranyl-methanol; In dichloromethane; at 0 ℃; for 0.166667h; With potassium fluoride; water; In dichloromethane; at 25 ℃; for 0.5h;	90.2 % Chromat. 9.8 % Chromat.