Welcome to LookChem.com Sign In|Join Free
  • or
Benzeneacetamide, N-(2-hydroxy-1,1-dimethylethyl)-, also known as 2-hydroxy-2-methylpropan-1-yl-benzeneacetamide, is an organic compound with the chemical formula C11H15NO2. It is a derivative of benzeneacetamide, featuring a 2-hydroxy-1,1-dimethylethyl group attached to the nitrogen atom. Benzeneacetamide, N-(2-hydroxy-1,1-dimethylethyl)- is characterized by its molecular weight of 191.24 g/mol and a melting point of 76-78°C. It is a colorless to pale yellow solid and is soluble in organic solvents such as ethanol and methanol. The compound has potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity.

1569-06-8

Post Buying Request

1569-06-8 Suppliers

Recommended suppliers

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

1569-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1569-06-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1569-06:
(6*1)+(5*5)+(4*6)+(3*9)+(2*0)+(1*6)=88
88 % 10 = 8
So 1569-06-8 is a valid CAS Registry Number.

1569-06-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1-hydroxy-2-methylpropan-2-yl)-2-phenylacetamide

1.2 Other means of identification

Product number -
Other names 2-Phenylacetamino-2-hydroxymethyl-propan

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:1569-06-8 SDS

1569-06-8Relevant academic research and scientific papers

Lanthanide catalyzed synthesis of β-hydroxyl amides

Zhou, Peiwen,Natale

, p. 3317 - 3330 (1998)

Lanthanide (III) chloride improved the reaction of carboxylic esters with β-amino alkoxides (generated in situ from β-amino alcohols) and produced β-hydroxyl amides under mild conditions, and in high yields.

?A!-annellated pyrrole derivatives and their use in pharmacology

-

, (2008/06/13)

The present invention relates to heterocyclic compounds with the formula STR1 in which R1 to R7, B, a, and X have the meanings indicated in the specification. These compounds can be used for the treatment of diseases of the rheumatic

A mild, nonacidic method for the conversion of carboxylic esters into oxazolines

Dodd,Guan,Schwender

, p. 1003 - 1008 (2007/10/02)

Conversion of carboxylic esters directly into amide alcohols is facilitated by use of base. Combined with a nonacidic cyclization of the intermediate amide alcohol this method allows formation of oxazolines under nonacidic conditions directly from the car

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1569-06-8