TERT-BUTYL 7-FORMYLINDOLINE-2-CARBOXYLATE

TERT-BUTYL 7-FORMYLINDOLINE-2-CARBOXYLATE - Names and Identifiers

Name	1-BOC-2,3-DIHYDRO-7-INDOLECARBALDEHYDE
Synonyms	N-Boc 7-formylindoline N-BOC-INDOLINE-7-CARBOXALDEHYDE N-BOC-2,3-dihydro-7-indolecarbalehyde 1-BOC-2,3-DIHYDRO-7-INDOLECARBALDEHYDE tert-butyl 7-forMylindoline-1-carboxylate TERT-BUTYL 7-FORMYL-1-INDOLINECARBOXYLATE TERT-BUTYL 7-FORMYLINDOLINE-2-CARBOXYLATE 1-(tert-Butoxycarbonyl)indoline-7-carboxaldehyde tert-butyl 7-formyl-2,3-dihydro-1H-indole-1-carboxylate tert-Butyl 7-formylindoline-1-carboxylate in stock Factory
CAS	174539-67-4
InChI	InChI=1/C14H17NO3/c1-14(2,3)18-13(17)15-8-7-10-5-4-6-11(9-16)12(10)15/h4-6,9H,7-8H2,1-3H3

TERT-BUTYL 7-FORMYLINDOLINE-2-CARBOXYLATE - Physico-chemical Properties

Molecular Formula	C14H17NO3
Molar Mass	247.29
Density	1.186g/cm³
Melting Point	86-90 °C
Boling Point	364.4°C at 760 mmHg
Flash Point	174.2°C
Vapor Presure	1.69E-05mmHg at 25°C
Storage Condition	under inert gas (nitrogen or Argon) at 2-8°C
Refractive Index	1.575

TERT-BUTYL 7-FORMYLINDOLINE-2-CARBOXYLATE - Risk and Safety

Hazard Symbols	T - Toxic
Risk Codes	25 - Toxic if swallowed
Safety Description	45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
UN IDs	UN 2811 6.1/PG 3
WGK Germany	3

TERT-BUTYL 7-FORMYLINDOLINE-2-CARBOXYLATE - Introduction

1-BOC-2, the full name of N-Boc-7-oxabicyclo[2.2.1]hept-5-en-3-ylmethanol, is an organic compound. The following is a description of its nature, use, formulation and safety information:

Nature:
1-BOC-2, is a white or yellowish solid with a distinctive odor. Its molecular formula is C16H21NO3 and its relative molecular mass is 275.34g/mol.

Use:
1-BOC-2, has a wide range of uses. One of the main uses is as an important intermediate in organic synthesis. It can be used to synthesize indoline derivatives, which have important application value in drug research and development and manufacturing.

Method: The preparation of
1-BOC-2, is generally achieved by chemical synthesis methods. A common method is to react 7-oxabicyclo[2.2.1]hept-5-ene with methanol, followed by an addition reaction of a protecting group, such as using a t-butoxycarbonyl(Boc) to protect the amine group.

Safety Information:
1-BOC-2, you need to pay attention to safety during storage and handling. It is irritating and harmful and may cause irritation and damage to the eyes, skin and respiratory tract. Appropriate personal protective equipment such as gloves, laboratory glasses and protective face masks should be worn during use. At the same time, it should be operated under well-ventilated conditions and away from fire and flammable materials.

Last Update：2024-04-09 21:11:58