BOC-ALGLY-(C*CH2)OH

BOC-ALGLY-(C*CH2)OH - Names and Identifiers

Name	Boc-(S)-3-Amino-5-hexenoic acid
Synonyms	BOC-ALGLY-(C*CH2)OH RARECHEM AK PT B009 Boc-b-HoGly(allyl)-OH BOC-BETA-HOGLY(ALLYL)-OH BOC-L-BETA-HOMOALLYLGLYCINE BOC-(S)-3-AMINO-5-HEXENOIC ACID Boc-(S)-3-Amino-5-hexenoic acid N-BETA-T-BUTOXYCARBONYL-L-HOMOALLYLGLYCINE N-T-BUTOXYCARBONYL-(S)-3-AMINO-5-HEXENOIC ACID
CAS	270263-03-1

BOC-ALGLY-(C*CH2)OH - Physico-chemical Properties

Molecular Formula	C11H19NO4
Molar Mass	229.27
Density	1.078
Boling Point	372.2±35.0 °C(Predicted)
BRN	9127734
pKa	4.43±0.10(Predicted)
Storage Condition	2-8°C

BOC-ALGLY-(C*CH2)OH - Risk and Safety

Hazard Symbols	Xn - Harmful
Risk Codes	R22 - Harmful if swallowed R36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S24/25 - Avoid contact with skin and eyes.
WGK Germany	3
HS Code	29241990
Hazard Class	IRRITANT

BOC-ALGLY-(C*CH2)OH - Introduction

Boc-(S)-3-Amino-5-hexenoic acid is an organic compound whose chemical formula is C12H21NO4. The following is a description of the properties, uses, preparation and safety information of the compound:

1. nature:
-Appearance: Boc-(S)-3-Amino-5-hexenoic acid is a solid, and the common form is white crystalline powder.
-Melting point: The compound has a melting point, and its specific value depends on the purity.
-Solubility: Boc-(S)-3-Amino-5-hexenoic acid is soluble in common organic solvents.

2. use:
-Synthetic intermediate: Boc-(S)-3-Amino-5-hexenoic acid is commonly used as a chemical synthesis intermediate and has important applications in pharmaceutical synthesis and organic synthesis.
-Functional group: Its pentenoic acid structure and amino group give the compound unique properties and can be used to prepare compounds with specific functions.
-Biological activity: Due to the special properties of its structure, the compound may have specific biological activities, such as antibacterial activity or anti-cancer activity.

3. preparation method:
- Boc-(S)-3-Amino-5-hexenoic acid can be prepared by organic synthesis reactions. A common method is to use the corresponding pentenal in the presence of an amino compound for addition reaction, And at the end of its acyl protection.

4. Safety Information:
- Boc-(S)-3-Amino-5-hexenoic acid is a chemical that must be operated under appropriate laboratory conditions.
-When using this compound, you must wear appropriate personal protective equipment, such as laboratory gloves and protective glasses.
-Avoid inhalation, ingestion and skin contact of the compound. In the process of operation, should follow the correct laboratory operating procedures and safe operation guidelines.
-In the event of an accident or discomfort after exposure to the compound, seek medical help immediately.

Last Update：2024-04-09 21:04:16