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Thermo Scientific Chemicals
(S)-(-)-1-Boc-3-aminopyrrolidine, 95%
CAS: 147081-44-5 | C9H18N2O2 | 186.26 g/mol
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化學識別
CAS147081-44-5
IUPAC Nametert-butyl 3-aminopyrrolidine-1-carboxylate
Molecular FormulaC9H18N2O2
InChI KeyCMIBWIAICVBURI-UHFFFAOYNA-N
SMILESCC(C)(C)OC(=O)N1CCC(N)C1
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規格
規格表
規格表Appearance (Color)Clear colorless to yellow
FormLiquid
Optical Rotation-3.1? ? 0.2? (neat)
Refractive Index1.4700-1.4740 @ 20?C
Assay (GC)≥94.0%
(S)-(-)-1-Boc-3-aminopyrrolidine is specifically used to protect amine in the solid phase synthesis of peptides. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals agrochemicals and dyestuff fields.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
(S)-(-)-1-Boc-3-aminopyrrolidine is specifically used to protect amine in the solid phase synthesis of peptides. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals agrochemicals and dyestuff fields.
Notes
Store under inert gas. It is sensitive to air. Store in a cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
(S)-(-)-1-Boc-3-aminopyrrolidine is specifically used to protect amine in the solid phase synthesis of peptides. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals agrochemicals and dyestuff fields.
Notes
Store under inert gas. It is sensitive to air. Store in a cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Jiwon Seo.; Pavel Martásek.; Linda J. Romanb.; Richard B. Silverman. Selective l-nitroargininylaminopyrrolidine and l-nitroargininylaminopiperidine neuronal nitric oxide synthase inhibitors. Bioorganic & Medicinal Chemistry. 2007, 15 (5), 1928-1938.
- Takaaki Sumiyoshi.; Takeshi Enomoto.; Kentaro Takai.; Yoko Takahashi.; Yasuko Konishi.; Yoshiharu Uruno.; Kengo Tojo.; Atsushi Suwa.; Harumi Matsuda.; Tomokazu Nakako.; Mutsuko Sakai.; Atsushi Kitamura.; Yasuaki Uematsu.; Akihiko Kiyoshi. Discovery of Novel N-Substituted Oxindoles as Selective M1 and M4 Muscarinic Acetylcholine Receptors Partial Agonists. ACS Med. Chem. Lett. 2013, 4 (2), 244-248.
- Product of Toray Industries, Inc.