Welcome to LookChem.com Sign In|Join Free

CAS

  • or

82004-45-3

β-Methoxyaminoisopropylmalonic acid diethyl ester is a chemical compound with the molecular formula C9H17NO5. It is an ester derivative of β-methoxyaminoisopropylmalonic acid, featuring a β-amino alcohol moiety and a malonic acid structure. β-methoxyaminoisopropylmalonic acid diethyl ester is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical properties. It can be synthesized through various methods, including the condensation of β-methoxyaminoisopropanol with diethyl malonate. The compound is typically a colorless liquid and is sensitive to hydrolysis, which can lead to the formation of the corresponding acid or alcohol under certain conditions. Its reactivity makes it a valuable building block in organic chemistry, particularly in the preparation of complex molecules that require the β-amino alcohol functionality.

82004-45-3

Post Buying Request

82004-45-3 Suppliers

Recommended suppliersmore

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

82004-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82004-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,0 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82004-45:
(7*8)+(6*2)+(5*0)+(4*0)+(3*4)+(2*4)+(1*5)=93
93 % 10 = 3
So 82004-45-3 is a valid CAS Registry Number.

82004-45-3Relevant articles and documents

ASYMMETRICAL NONBRIDGEHEAD NITROGEN-XXVI SYNTHESIS, CONFIGURATIONALSTABILITY, AND RESOLUTION OF N,N-DIALKOXYAMINES INTO ANTIPODES

Konstyanovsky, Remir G.,Rudchenko, Vladimir F.,Shtamburg, Vasilii G.,Chervin, Ivan I.,Nasibov, Shahin S.

, p. 4245 - 4254 (1981)

Alkoxyamines with tertiary N-alkyl substituents were chlorinated to N-chloro-N-alkoxyamines whose reaction with alcohols enabled synthesis of N,N-dialkoxyamines.The DNMR method wos used to determine the barriers of of inversion of these compounds.Alkaline hydrolysis (13) followed by subsequent reactions with R-(+)- and S-(-)-a-phenylethylamine yielded diastereomeric salt (+29 and -29) whose crystallization and subsequent esterification resulted in optically active acyclic amines (-13 and +13) with the asymmetric center only at the N atom in the open chain.

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

What can I do for you?
Get Best Price

Get Best Price for 82004-45-3