160256-75-7

Basic information

• Product Name: DIBENZYL 2,2'-IMINOBIS(ETHYLCARBAMATE)
• Synonyms: N,N''-DI-BENZYLOXYCARBONYL-DIETHYLENETRIAMINE;N,N''-DI-Z-DIETHYLENETRIAMINE;Z-EDA-EDA-Z;DIBENZYL 2,2'-IMINOBIS(ETHYLCARBAMATE);Dibenzyl (azanediylbis(ethane-2,1-diyl))dicarbamate;N,N''-Di-Z-diethylenetriamine≥ 97% (HPLC)
• CAS NO: 160256-75-7
• Molecular Formula: C₂₀H₂₅N₃O₄
• Molecular Weight: 371.43
• Mol File: 160256-75-7.mol
• Article Data: 15

Chemical Properties

• Melting Point: 70-74 °C
• Appearance: /
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• BRN: 7083538
• CAS DataBase Reference: DIBENZYL 2,2'-IMINOBIS(ETHYLCARBAMATE)(CAS DataBase Reference)
• NIST Chemistry Reference: DIBENZYL 2,2'-IMINOBIS(ETHYLCARBAMATE)(160256-75-7)
• EPA Substance Registry System: DIBENZYL 2,2'-IMINOBIS(ETHYLCARBAMATE)(160256-75-7)

Safety Data

• Hazard Codes: Xi,N
• Statements: 37/38-41-50
• Safety Statements: 26-39-61
• RIDADR: UN 3077 9/PG 3
• WGK Germany: 3
• Hazardous Substances Data: 160256-75-7(Hazardous Substances Data)

Usage

Description

DIBENZYL 2,2'-IMINOBIS(ETHYLCARBAMATE) is an organic compound that serves as a valuable building block in the synthesis of various chemical libraries. It is characterized by its off-white solid appearance and plays a crucial role in introducing a protected 2,2'-iminodi(ethylamine) scaffold in these libraries.

Uses

Used in Chemical Synthesis:
DIBENZYL 2,2'-IMINOBIS(ETHYLCARBAMATE) is used as a building block for the creation of chemical libraries. It is particularly useful in introducing a protected 2,2'-iminodi(ethylamine) scaffold, which can be further modified or functionalized to develop a wide range of compounds with diverse applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, DIBENZYL 2,2'-IMINOBIS(ETHYLCARBAMATE) is used as a key intermediate in the synthesis of various drug candidates. Its ability to introduce a protected 2,2'-iminodi(ethylamine) scaffold allows for the development of novel compounds with potential therapeutic applications.
Used in Research and Development:
DIBENZYL 2,2'-IMINOBIS(ETHYLCARBAMATE) is also utilized in research and development settings, where it aids in the exploration of new chemical reactions and the synthesis of innovative molecules. Its role in introducing a protected 2,2'-iminodi(ethylamine) scaffold makes it a valuable tool for scientists working on the design and development of new chemical entities.

Upstream product

• 13139-17-8 N-(Benzyloxycarbonyloxy)succinimide 
• 111-40-0 3-azapentane-1,5-diamine 
• 28170-07-2 benzyl phenyl carbonate 
• 5532-86-5 benzyl cyanoformate 
• 22129-07-3 N-benzyloxycarbonylimidazole 
• 100-51-6 benzyl alcohol 

Downstream Products

• 192636-10-5 N,N-Bis-(2-benzyloxycarbonylamino-ethyl)-succinamic acid 
• 236115-85-8 [2-((2-Benzyloxycarbonylamino-ethyl)-{2-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-ethyl}-amino)-ethyl]-carbamic acid benzyl ester 
• 344779-95-9 Acetic acid (1S,2S,3R,4S,6R)-4,6-bis-benzyloxycarbonylamino-2-{2-[bis-(2-benzyloxycarbonylamino-ethyl)-amino]-ethoxy}-3-((2S,3R,4R,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-3-benzyloxycarbonylamino-tetrahydro-pyran-2-yloxy)-cyclohexyl ester 
• 174700-73-3 [bis[2-(benzyloxycarbonylamino)ethyl]amino]acetic acid tert-butyl ester 
• 872462-43-6 (5-benzyloxycarbonylamino-6-(bis-(2-benzyloxycarbonylaminoethyl)-amino)-hexyl)-carbamic acid tert-butyl ester 
• 1020857-61-7 4-benzyloxycarbonylamino-5-(bis-(2-benzyloxycarbonylaminoethyl)-amino)-pentanoic acid benzyl ester 
• 872462-22-1 (4-(2-benzyloxycarbonylamino-3-(bis-(2-benzyloxycarbonylaminoethyl)-amino)-propyl)-phenoxy)-acetic acid benzyl ester 
• 1083175-01-2 tert-butyl (2S)-5-[bis(2-{[(benzyloxy)carbonyl]amino}ethyl)amino]-2-{bis[(tert-butoxy)carbonyl]amino}pentanoate 
• 1145787-27-4 N'-uracil-3-ylaminocarbonylmethyl-N,N''-dicarbobenzoxydiethylenetriamine 
• 1245573-65-2 C₃₇H₄₆BF₂N₅O₄ 
• 1333174-04-1 2-N,N-bis(2-CBz-aminoethyl)amino-4,6-dichloro-1,3,5-triazine 
• 1333174-03-0 2-N,N-bis(2-CBz-aminoethyl)amino-4,6-bis(N-propylamino)-1,3,5-triazine 
• 1571097-22-7 dibenzyl (((tert-butoxycarbonyl)azanediyl)bis(ethane-2,1-diyl))dicarbamate 
• 1610625-57-4 N,N′′-bis(carbobenzyloxy)-N′-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]bis(2-aminoethyl)amine 

Relevant articles and documents

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Single-molecule fluorescence microscopy provided information about the real-time distribution of chemical reactivity on silicon oxide supports at the solution-surface interface, at a level of detail which would be unavailable from a traditional ensemble technique or from a technique that imaged the static physical properties of the surface. Chemical reactions on the surface were found to be uncorrelated; that is, the chemical reaction of one metal complex did not influence the location of a future chemical reaction of another metal complex.

INSULIN DERIVATIVES CONJUGATED WITH STRUCTURALLY WELL DEFINED BRANCHED POLYMERS

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