N-Boc-Ethylenediamine

N-Boc-Ethylenediamine Basic information

Product Name:	N-Boc-Ethylenediamine
Synonyms:	1-BOC-ETHYLENEDIAMINE;1-BOC-AMINO-1,2-ETHANEDIAMINE;AKOS 91563;N-TERT-BUTOXYCARBONYL-ETHYLENEDIAMINE;N-TERT-BUTYLOXYCARBONYL-ETHYLENEDIAMINE;n-tert-butyloxycarbonyl-1,2-ethylenediamine;N-BOC-1,2-DIAMINOETHANE;BUTTPARK 27\08-29
CAS:	57260-73-8
MF:	C7H16N2O2
MW:	160.21
EINECS:	611-490-6
Product Categories:	Exciton Chirality CD Methodfor (for Monofunctional Compounds);Monoprotected Diaminoalkanes;N-Boc-diaminoalkanes;Absolute Configuration Determination (Exciton Chirality CD Method);Analytical Chemistry;Enantiomer Excess & Absolute Configuration Determination;Cross Linking Reagents;Aliphatics;Nitric Oxide Reagents;Amines and Anilines;N-BOC;Amines;blocks
Mol File:	57260-73-8.mol

N-Boc-Ethylenediamine Chemical Properties

Boiling point	72-80 °C0.1 mm Hg(lit.)
density	1.012 g/mL at 20 °C(lit.)
refractive index	n20/D 1.458(lit.)
Fp	>230 °F
storage temp.	Keep in dark place,Inert atmosphere,2-8°C
solubility	Chloroform (Slightly), Methanol (Slightly)
pka	12.40±0.46(Predicted)
form	Oily Liquid
Specific Gravity	1.012
color	Clear colorless to very light yellow
Water Solubility	Miscible with methanol and chloroform. Slightly miscible with water.
Sensitive	Air Sensitive
BRN	1932330
Exposure limits	ACGIH: TWA 100 ppm OSHA: TWA 100 ppm(300 mg/m3) NIOSH: IDLH 1600 ppm; TWA 100 ppm(300 mg/m3); STEL 150 ppm(450 mg/m3)
InChIKey	AOCSUUGBCMTKJH-UHFFFAOYSA-N
CAS DataBase Reference	57260-73-8(CAS DataBase Reference)

Safety Information

Hazard Codes	C
Risk Statements	34
Safety Statements	26-36/37/39-45
RIDADR	UN 2735 8/PG 3
WGK Germany	3
F	10-34
Hazard Note	Corrosive/Air Sensitive
HazardClass	8
PackingGroup	III
HS Code	29241990

MSDS Information

Provider	Language
SigmaAldrich	English
ALFA	English

N-Boc-Ethylenediamine Usage And Synthesis

Chemical Properties	Clear colorless to very light yellow oily liquid
Uses	suzuki reaction
Uses	N-Boc-ethylenediamine is used in the synthesis of thyronamine derivatives. It is also used in the preparation of (2-isothiocyanato-ethyl)-carbamic acid tert-butyl ester by reacting with carbon disulfide. Further, it is used in both oligonucleotide and peptide synthesis.
Uses	N-Boc-ethylenediamine is used in the synthesis of Thyronamine derivatives and analogs.

N-Boc-Ethylenediamine Preparation Products And Raw materials

Raw materials	Ethanol-->Sodium hydroxide-->Hydrochloric acid-->Methanol-->Dichloromethane-->Acetic acid-->Chloroform-->Di-tert-butyl dicarbonate-->Ethylenediamine-->1,3-Diaminopropane
Preparation Products	LAZABEMIDE-->H-(2S,4R)-(4-OCO-NH-CH2-CH2-NH-Boc)-Pro-OH-->ETHYL [2-(BOC-AMINO)ETHYLAMINO]ACETATE HYDROCHLORIDE-->biotinylamidoethylacetamide-->FMOC-L-HYP(BOM)-OH-->TERT-BUTYL N-(2-ISOTHIOCYANATOETHYL)CARBAMATE

Boc-Aib-OH N-Boc-(2R,3R,4S)-dolaproine TERT-BUTYL N-(2-HYDROXYETHYL)CARBAMATE N-Boc-endo-3-aminotropane N-Boc-exo-3-aminotropane N-Boc-3-piperidineacetic acid N-Boc-L-trans-4,5-Methanoproline BOC-METYR(ME)-OH DCHA t-butyl chloroformate Cyhalofop-butyl N-BOC-ETHYLENEDIAMINE HCL,N-BOC-ETHYLENEDIAMINE HYDROCHLORIDE,N-T-BOC-ETHYLENEDIAMINE HCL POLYURETHANE N-Cbz-N'-Boc-ethylenediamine 2-(2-Aminoethylamino)ethanol Buprofezin tert-Butyl 4-aminobenzoate BUTYL OLEATE tert-Butyl glycinate

Email:[email protected] [email protected]

Copyright © 2024 Mywellwork.com All rights reserved.