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N-BOC-2-(2-AMINO-ETHOXY)-ETHYLAMINE structure, CAS 127828-22-2

N-BOC-2-(2-AMINO-ETHOXY)-ETHYLAMINE

CAS Number127828-22-2

SynonymsAmbotzPEG1067; 1-t-butoxycarbonylamino-3-oxa-pentan-5-amine; N-Boc-2-(2-amino-ethoxy)-ethylamine; tert-butyl 2-(2-aminoethoxy)ethylcarbamate; N-(tert-butyloxycarbonyl)-2,2'-oxybis(ethylamine); 5-(tert-butyloxycarbonylamino)-3-oxa-pentyl amine; N-t-butoxycarbonyl-3-oxa-1,5-pentanediamine; tert-Butyl [2-(2-aminoethoxy)ethyl]carbamate

Molecular FormulaC9H20O3N2

Molecular Weight204.27

Purity98%

Density1.024g/cm3

Boiling Point321.128ºC at 760 mmHg

Melting Point

Flash Point

AppearanceLiquid;Colorless to Light orange to Yellow clear liquid

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MSDSChineseEnglish

Symbol

Signal Word

Cat. No.: 2A-9060991 Purity: 98%
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Quality Control of [ 127828-22-2 ] Purity: 98% SDS Specification MoL

Chemical & Physical Properties
CAS Number127828-22-2
Catalog No.2A-9060991
Chinese Name[2-(2-氨基乙氧基)乙基]氨基甲酸叔丁酯
SynonymsAmbotzPEG1067; 1-t-butoxycarbonylamino-3-oxa-pentan-5-amine; N-Boc-2-(2-amino-ethoxy)-ethylamine; tert-butyl 2-(2-aminoethoxy)ethylcarbamate; N-(tert-butyloxycarbonyl)-2,2'-oxybis(ethylamine); 5-(tert-butyloxycarbonylamino)-3-oxa-pentyl amine; N-t-butoxycarbonyl-3-oxa-1,5-pentanediamine; tert-Butyl [2-(2-aminoethoxy)ethyl]carbamate
Molecular FormulaC9H20O3N2
Molecular Weight204.27
Purity98
Density1.024g/cm3
Boiling Point321.128ºC at 760 mmHg
AppearanceLiquid;Colorless to Light orange to Yellow clear liquid
Water SolubilitySoluble (53 g/L) (25 ºC)
Storage ConditionStore under inert gas; avoid air
ApplicationAmino-PEG2-NH-Boc is a PEG-based PROTAC bridge used to synthesize PROTAC.
HTC2924199090
MDL NumberMFCD12031501
SMILESCC(C)(C)OC(=O)NCCOCCN
InChI KeyVULKFBHOEKTQSF-UHFFFAOYSA-N
MSDSmsds/60991_1_127828_22_2.pdf
Use ofAmino-PEG2-NH-Boc is a PEG-based PROTAC linker can be used in the synthesis of PROTACs[1]. Properties Name tert-butyl N-[2-(2-aminoethoxy)ethyl]carbamate Synonym More Synonyms Amino-PEG2-NH-Boc Biological Activity Description Amino-PEG2-NH-Boc is a PEG-based PROTAC linker can be used in the synthesis of PROTACs[1]. Related Catalog Research Areas >> Cancer Signaling Pathways >> PROTAC >> PROTAC Linker Alkyl/ether In Vitro PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins. References [1]. Qiu X, et al. Chemoselective Synthesis of Lenalidomide-Based PROTAC Library Using Alkylation Reaction. Org Lett. 2019 May 17;21(10):3838-3841. Chemical & Physical Properties Molecular Formula C9H20N2O3 Exact Mass 204.14700 PSA 77.07000 LogP 1.39110 Index of Refraction 1.457 InChIKey VULKFBHOEKTQSF-UHFFFAOYSA-N SMILES CC(C)(C)OC(=O)NCCOCCN Safety Information Hazard Codes Xi HS Code 2924199090 Synthetic Route CAS#:176220-30-7 Amino-PEG2-NH-Boc CAS#:127828-22-2 Literature: EP1745802 A1, ; Page/Page column 17 ; Di-tert-butyl d... CAS#:24424-99-5 2,2'-Oxydiethan... CAS#:60792-79-2 Amino-PEG2-NH-Boc CAS#:127828-22-2 Literature: Journal of Organic Chemistry, , vol. 72, # 7 p. 2289 - 2296 2,2-Oxybis(ethy... CAS#:2752-17-2 Di-tert-butyl d... CAS#:24424-99-5 Amino-PEG2-NH-Boc CAS#:127828-22-2 Literature: Tetrahedron Letters, , vol. 47, # 17 p. 2915 - 2919 Precursor & DownStream Precursor 6 CAS#:24424-99-5 Di-tert-butyl d... CAS#:60792-79-2 2,2'-Oxydiethan... CAS#:2752-17-2 2,2-Oxybis(ethy... CAS#:1046804-80-1 Tert-butyl 2-(2... DownStream 0
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 30.0%
Transport InfoProduct name: Summary 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
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