Welcome to LookChem.com Sign In|Join Free
  • or
(+/-)-trans-3,4-dimethyl-1-(phenylmethyl)-azitidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87568-35-2

Post Buying Request

87568-35-2 Suppliers

Recommended suppliers

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

87568-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87568-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,6 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87568-35:
(7*8)+(6*7)+(5*5)+(4*6)+(3*8)+(2*3)+(1*5)=182
182 % 10 = 2
So 87568-35-2 is a valid CAS Registry Number.

87568-35-2Relevant academic research and scientific papers

A One-Pot Conversion of an Aziridine to a β-Lactam using Nickel Tetracarbonyl

Chamchaang, Wilaiporn,Pinhas, Allan R.

, p. 710 - 711 (1988)

A one-pot, inert atmosphere conversion of an aziridine to a β-lactam has been achived, using nickel tetracarbonyl, in which the less substituted C-N bond is carbonylated.

The Conversion of an Aziridine to a β-Lactam

Chamchaang, Wilaiporn,Pinhas, Allan R.

, p. 2943 - 2950 (2007/10/02)

A one-pot, inert atmosphere conversion of an aziridine to a β-lactam using nickel tetracarbonyl as the carbonyl source is described.In this reaction it is the less substituted carbon-nitrogen bond which is carbonylated.The proposed mechanism for this reac

STEREOSELECTIVE CONJUGATE ADDITION - ALKYLATIONS OF α,β-UNSATURUTED IRON ACYLS

Liebeskind, Lanny S.,Welker, Mark E.

, p. 3079 - 3082 (2007/10/02)

Conjugate addition and conjugate addition-alkylations proceed with very high stereoselectivity to α,β-unsaturated acyls of η5-CpFe(CO)(PPh3).Oxidative cleavage of the products provides high yields of organic acid derivatives (esters, β-lactams)

Synthesis of β-lactam antibiotics by the sulfeno-cycloamination

Ihara,Haga,Yonekura,et al.

, p. 7345 - 7352 (2007/10/02)

A novel efficient beta -lactam synthesis was achieved by two successive processes (sulfeno-cycloamination), addition of phenysulfenyl chloride to alpha , beta -unsaturated amides followed by base treatment. Key synthetic intermediates of monobactams and nocardicin derivatives were obtained via this method. construction of the 1-carbapenam ring system by the sulfenocycloamination is also described.

NOVEL STEREOSELECTIVE SYNTHESIS OF β-LACTAMS VIA EPISULFONIUM ION INTERMEDIATE

Ihara, Masataka,Fukumoto, Keiichiro

, p. 1435 - 1438 (2007/10/02)

A number of monocyclic β-lactams were synthesized by addition of benzenesulfonyl chloride to α,β-unsaturated olefins followed by base treatment in the presence of a phase transfer catelyst.The cyclization proceeds in a stereoselective manner most probably

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 87568-35-2