17136-37-7

Basic information

• Product Name: DIETHYL BENZYLIMINODIACETATE 97
• Synonyms: DIETHYL BENZYLIMINODIACETATE 97;Diethyl benzyliminodiacetate 97%
• CAS NO: 17136-37-7
• Molecular Formula: C₁₅H₂₁NO₄
• Molecular Weight: 279.334
• Product Categories: C12 to C63;Carbonyl Compounds;Esters
• Mol File: 17136-37-7.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 324-325 °C(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 1.076 g/mL at 25 °C(lit.)
• Vapor Pressure: 2.14E-05mmHg at 25°C
• Refractive Index: n20/D 1.4930(lit.)
• CAS DataBase Reference: DIETHYL BENZYLIMINODIACETATE 97(CAS DataBase Reference)
• NIST Chemistry Reference: DIETHYL BENZYLIMINODIACETATE 97(17136-37-7)
• EPA Substance Registry System: DIETHYL BENZYLIMINODIACETATE 97(17136-37-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 17136-37-7(Hazardous Substances Data)

Usage

General Description

DIETHYL BENZYLIMINODIACETATE 97 is a chemical compound with the molecular formula C15H25NO4. It is a derivative of benzylamine and is commonly used as a fragrance ingredient in the manufacturing of perfumes, soaps, and cosmetics. It has a light, fresh, and floral scent and is often added to formulations for its pleasant aroma. Additionally, it can act as a stabilizer and fixative in fragrance products, helping to prolong the scent's longevity. As a high-purity compound, DIETHYL BENZYLIMINODIACETATE 97 is suitable for use in various personal care and household products.

InChI:InChI=1/C15H21NO4/c1-3-19-14(17)11-16(12-15(18)20-4-2)10-13-8-6-5-7-9-13/h5-9H,3-4,10-12H2,1-2H3

Upstream product

• 105-39-5 chloroacetic acid ethyl ester 
• 100-46-9 benzylamine 
• 623-73-4 diazoacetic acid ethyl ester 
• 105-36-2 ethyl bromoacetate 
• 6290-05-7 Diethyl iminodiacetate 
• 100-39-0 benzyl bromide 
• 6436-90-4 ethyl 2-(benzylamino)acetate 

Downstream Products

• 376395-32-3 diethyl 1-benzyl-3,4-dihydroxy-1H-pyrrole-2,5-dicarboxylate 
• 112193-82-5 4-benzyl-1,4,7,10-tetraazacyclododecane-2,6-dione 
• 101-32-6 N-benzyl-diethanolamine 
• 1138458-07-7 N-benzyl-3,3,5,5-d₄-morpholine 
• 1138458-06-6 2,2'-(benzylimino)bis(1,1-d₂-ethanol) 

Relevant articles and documents

Cosmosen: Octa-Armed 24-Membered Cyclic Octaamine Synthesized from a Byproduct in the Preparation of 4-Benzyl-2,6-dioxocyclen

The synthesis of an octa-armed 24-membered cyclic octaamine (1) is reported. When 4-benzyl-1,4,7,10-tetraazacyclododecane-2,6-dione (3a) was prepared by the reaction of diethylenetriamine with diethyl N-benzyliminodiacetate (2), a dimeric macrocycle (3b) was obtained as a byproduct in a 5% yield. An octa-armed 24-membered cyclic octaamine (1), named Cosmosen, was prepared via the reductive amination and reduction of 3b. The binding constants for the 1:1 and 2:1 (Ag+/1) complexation of 1 were estimated to be ca. 7.9 and 13.9, respectively, by titration experiments using UV-vis spectrometry in methanol and chloroform (v/v, 9:1) solutions at 298 K.

COMPOSITIONS AND METHODS FOR THE TREATMENT OF VIRAL INFECTIONS

Compositions and methods for the treatment of viral infections include conjugates containing inhibitors of viral neuraminidase (e.g., zanamivir, peramivir, or analogs thereof) linked to an Fc monomer, an Fc domain, and Fc-binding peptide, an albumin protein, or albumin-binding peptide. In particular, conjugates can be used in the treatment of viral infections (e.g., influenza viral infections).

Lanthanum(III) triflate catalyzed direct amidation of esters

Lanthanum trifluoromethanesulfonate is an effective single-component catalyst for synthesizing a variety of amides directly from esters and amines under mild conditions. Highly selective amidation of esters and amines, as well as catalyst-controlled amidation of esters, demonstrated the effectiveness of the catalyst system.