Carbamic acid, N-(4-iodophenyl)-, 1,1-dimethylethyl ester
TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE
CAS: 159217-89-7
Molecular Formula: C11H14INO2
Carbamic acid, N-(4-iodophenyl)-, 1,1-dimethylethyl ester - Names and Identifiers
| Name | TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE |
| Synonyms | N-Boc 4-iodoaniline N-BOC-4-IODOANILINE TERT-BUTYL 4-IODOPHENYLCARBAMATE TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE N-(tert-Butoxycarbonyl)-4-iodoaniline (4-Iodophenyl)carbamic acid tert-butyl ester N-(4-iodophenyl)carbamic acid tert-butyl ester Carbamic acid, N-(4-iodophenyl)-, 1,1-dimethylethyl ester |
| CAS | 159217-89-7 |
| InChI | InChI=1/C11H14INO2/c1-11(2,3)15-10(14)13-9-6-4-8(12)5-7-9/h4-7H,1-3H3,(H,13,14) |
Carbamic acid, N-(4-iodophenyl)-, 1,1-dimethylethyl ester - Physico-chemical Properties
| Molecular Formula | C11H14INO2 |
| Molar Mass | 319.14 |
| Density | 1.591±0.06 g/cm3(Predicted) |
| Melting Point | 144-148 °C |
| Boling Point | 299.0±23.0 °C(Predicted) |
| Flash Point | 134.6°C |
| Vapor Presure | 0.00123mmHg at 25°C |
| pKa | 13.12±0.70(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Sensitive | Light Sensitive |
| Refractive Index | 1.604 |
| MDL | MFCD03490497 |
| Physical and Chemical Properties | Sensitivity: Light Sensitive |
Carbamic acid, N-(4-iodophenyl)-, 1,1-dimethylethyl ester - Risk and Safety
| Risk Codes | R22 - Harmful if swallowed R43 - May cause sensitization by skin contact R50 - Very Toxic to aquatic organisms |
| Safety Description | S36/37 - Wear suitable protective clothing and gloves. S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. |
| UN IDs | UN 3077 9 / PGIII |
| WGK Germany | 3 |
Carbamic acid, N-(4-iodophenyl)-, 1,1-dimethylethyl ester - Introduction
TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE is an organic compound whose Properties, Uses, preparation and safety information are as follows:
Nature:
TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE is a white solid with a special smell. Its chemical formula is C12H14INO2 and its relative molecular mass is 307.15g/mol. The compound has good stability and is soluble in common organic solvents and acids.
Use:
TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE is a common intermediate in organic synthesis. It can be used to prepare various drugs, pesticides and bioactive molecules, and has a wide range of applications.
Method:
The preparation of TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE is usually carried out by the following steps:
1. 4-iodoaniline reacts with dimethyl sulfoxide (DMSO) to generate a substrate.
2. Under alkaline conditions, Boc2O (tert-butoxycarbonyl oxalyl chloride) is added to react to obtain the target product TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE.
Safety Information:
TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE is an organic substance and needs to be operated under correct laboratory conditions. The following is the safety information to note:
1. Wear protective goggles, gloves, and a lab coat to ensure adequate ventilation when handling the compound.
2. Avoid contact with skin, eyes and respiratory system, so as not to cause irritation or other adverse reactions.
3. When storing, keep the TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE in an airtight container, away from open flames or heat sources.
4. When handling this compound, it is necessary to follow correct waste disposal measures and comply with local regulations.
Please note that this information is for reference only. Please ensure that you obtain correct laboratory instructions and follow laboratory safety regulations before performing any chemical experiments.
Nature:
TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE is a white solid with a special smell. Its chemical formula is C12H14INO2 and its relative molecular mass is 307.15g/mol. The compound has good stability and is soluble in common organic solvents and acids.
Use:
TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE is a common intermediate in organic synthesis. It can be used to prepare various drugs, pesticides and bioactive molecules, and has a wide range of applications.
Method:
The preparation of TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE is usually carried out by the following steps:
1. 4-iodoaniline reacts with dimethyl sulfoxide (DMSO) to generate a substrate.
2. Under alkaline conditions, Boc2O (tert-butoxycarbonyl oxalyl chloride) is added to react to obtain the target product TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE.
Safety Information:
TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE is an organic substance and needs to be operated under correct laboratory conditions. The following is the safety information to note:
1. Wear protective goggles, gloves, and a lab coat to ensure adequate ventilation when handling the compound.
2. Avoid contact with skin, eyes and respiratory system, so as not to cause irritation or other adverse reactions.
3. When storing, keep the TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE in an airtight container, away from open flames or heat sources.
4. When handling this compound, it is necessary to follow correct waste disposal measures and comply with local regulations.
Please note that this information is for reference only. Please ensure that you obtain correct laboratory instructions and follow laboratory safety regulations before performing any chemical experiments.
Last Update：2024-04-09 19:05:46
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CAS: 159217-89-7
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CAS: 159217-89-7
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
View History
Carbamic acid, N-(4-iodophenyl)-, 1,1-dimethylethyl ester
2-甲基磺酰基-5-氯嘧啶-4-甲酸
Anti-USP5 Polyclonal Antibody
2-甲基磺酰基-5-氯嘧啶-4-甲酸
Anti-USP5 Polyclonal Antibody