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Shanghai Carlow Chemicals Co., Ltd.
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21-33526724 18930996265 |
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Product Name:tert-Butyl N-[1-(2-aminoethyl)cyclopropyl]carbamate CAS:753023-60-8 Purity:97% NMR Package:10G;100G
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Tcichem, Inc.
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13918644899 |
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tianchong009@hotmail.com |
Products Intro: |
Product Name:tert-butyl 1-(2-aminoethyl)cyclopropylcarbamate CAS:753023-60-8 Purity:95% HPLC Package:1G;5G;10G;25G;50G;100G;1KG
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Aikon International Limited
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025-66113011 18112977050 |
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sales01@aikonchem.com |
Products Intro: |
Product Name:tert-Butyl N-[1-(2-aminoethyl)cyclopropyl]carbamate CAS:753023-60-8 Purity:95+% Package:1g;5g;10g
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| tert-Butyl (1-(2-aminoethyl)cyclopropyl)carbamate Basic information |
Product Name: | tert-Butyl (1-(2-aminoethyl)cyclopropyl)carbamate | Synonyms: | Carbamic acid, [1-(2-aminoethyl)cyclopropyl]-, 1,1-dimethylethyl ester (9CI); Carbamic acid, [1-(2-aminoethyl)cyclopropyl]-, 1,1-dimethylethyl ester;tert-butyl 1-(2-aminoethyl)cyclopropylcarbamate;tert-butyl N-[1-(2-aminoethyl)cyclopropyl]carbamate;1-(2-Amino-ethyl)-cyclopropyl]-carbamic acid tert-butyl ester;Carbamic acid, N-[1-(2-aminoethyl)cyclopropyl]-, 1,1-dimethylethyl ester;1-(2-Aminoethyl)-N-Boc-cyclopropanamine;tert-Butyl(1-(2-aminoethyl)cyclopropyl)aminocarbamate | CAS: | 753023-60-8 | MF: | C10H20N2O2 | MW: | 200.28 | EINECS: | | Product Categories: | N-BOC | Mol File: | 753023-60-8.mol | ![tert-Butyl (1-(2-aminoethyl)cyclopropyl)carbamate Structure](CAS/GIF/753023-60-8.gif) |
| tert-Butyl (1-(2-aminoethyl)cyclopropyl)carbamate Chemical Properties |
Boiling point | 299.9±9.0 °C(Predicted) | density | 1.04±0.1 g/cm3(Predicted) | pka | 12.79±0.20(Predicted) |
| tert-Butyl (1-(2-aminoethyl)cyclopropyl)carbamate Usage And Synthesis |
Uses | Tert-Butyl (1-(2-aminoethyl)cyclopropyl)carbamate, also known as carbamic acid, [1-(cyclopropylamino)ethyl]-, 1,1-dimethylethyl ester, is belongs to the class of carbamates, which are derivatives of carbamic acid. Carbamates have a wide range of applications, including as pesticides, herbicides, and fungicides. | Preparation | Tert-butyl 1-[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethyl]cyclopropylcarbamate (4.57g, 13.83 mmol) was added to ethanol (80 ml). Followed by adding 3.36ml (69.16 mmol) of hydrazine hydrate and the resulting mixture was heated under reflux for 16h. The mixture was filtered and washed with diethyl ether. Finally, the filtrate was evaporated to dryness to give 2.3g of tert-Butyl (1-(2-aminoethyl)cyclopropyl)carbamate as an orange oil.
![tert-Butyl (1-(2-aminoethyl)cyclopropyl)carbamate tert-Butyl (1-(2-aminoethyl)cyclopropyl)carbamate](/NewsImg/2023-10-16/6383306065439653863329980.jpg) | Origin | Tert-Butyl (1-(2-aminoethyl)cyclopropyl)carbamate (TAC) was first synthesized by researchers at the University of California, Los Angeles in 2006. The synthesis of TAC involved the reaction of tert-butyl carbamate with cyclopropylamine. |
| tert-Butyl (1-(2-aminoethyl)cyclopropyl)carbamate Preparation Products And Raw materials |
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