Boc-D-Cys(Trt)-OH Boc-S-trityl-D-cysteine
Boc-S-trityl-D-cysteine
CAS: 87494-13-1
Molecular Formula: C27H29NO4S
Boc-D-Cys(Trt)-OH Boc-S-trityl-D-cysteine - Names and Identifiers
| Name | Boc-S-trityl-D-cysteine |
| Synonyms | Boc-Cys(trt)-OH Boc-D-Cys(Trt)-OH Boc-S-trityl-D-cysteine (Tert-Butoxy)Carbonyl D-Cys(Trt)-OH Boc-D-Cys(Trt)-OH Boc-S-trityl-D-cysteine N-alpha-t-Butyloxycarbonyl-S-trityl-D-cysteine (S)-2-(Tert-butoxycarbonylamino)-3-(tritylthio)propanoic acid |
| CAS | 87494-13-1 |
| InChI | InChI=1/C27H29NO4S/c1-26(2,3)32-25(31)28(23(19-33)24(29)30)27(20-13-7-4-8-14-20,21-15-9-5-10-16-21)22-17-11-6-12-18-22/h4-18,23,33H,19H2,1-3H3,(H,29,30)/t23-/m1/s1 |
Boc-D-Cys(Trt)-OH Boc-S-trityl-D-cysteine - Physico-chemical Properties
| Molecular Formula | C27H29NO4S |
| Molar Mass | 463.59 |
| Density | 1.200±0.06 g/cm3(Predicted) |
| Melting Point | 146-149°C |
| Boling Point | 610.9±55.0 °C(Predicted) |
| Solubility | Chloroform (Slightly), DMSO (Slightly), Ethanol (Sparingly) |
| Appearance | Solid |
| Color | White to Off-White |
| pKa | 3.82±0.10(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,2-8°C |
| Refractive Index | 1.599 |
Boc-D-Cys(Trt)-OH Boc-S-trityl-D-cysteine - Introduction
Boc-S-trityl-D-cysteine is an organic compound with a chemical formula of C43H41NO4S and a molecular weight of 671.87. It contains a protecting group 4-tert-butoxycarbonyl (Boc), a trityl group and a D-cysteine residue.
Boc-S-trityl-D-cysteine is often used as a protecting group for amino acid derivatives in organic synthesis. It can protect the thiol group of cysteine to avoid non-specific reactions with other functional groups. In the synthesis of polypeptides, proteins, and other organic molecules, it is often used to protect the cysteine function in order to carry out deprotection reactions when appropriate.
The preparation method of the Boc-S-trityl-D-cysteine is to react 3-tert-butoxycarbonyl benzoic acid and DTNB (5,5 '-sodium dithiophenate) together to generate a compound, and then obtain the target product by hydrogenation reduction.
Regarding safety information, the toxicity of Boc-S-trityl-D-cysteine is low, but appropriate safety measures should be taken during operation. It may be irritating to the eyes, skin, and respiratory system, so contact should be avoided. Wear appropriate protective equipment such as lab gloves, glasses and laboratory goggles during use.
Boc-S-trityl-D-cysteine is often used as a protecting group for amino acid derivatives in organic synthesis. It can protect the thiol group of cysteine to avoid non-specific reactions with other functional groups. In the synthesis of polypeptides, proteins, and other organic molecules, it is often used to protect the cysteine function in order to carry out deprotection reactions when appropriate.
The preparation method of the Boc-S-trityl-D-cysteine is to react 3-tert-butoxycarbonyl benzoic acid and DTNB (5,5 '-sodium dithiophenate) together to generate a compound, and then obtain the target product by hydrogenation reduction.
Regarding safety information, the toxicity of Boc-S-trityl-D-cysteine is low, but appropriate safety measures should be taken during operation. It may be irritating to the eyes, skin, and respiratory system, so contact should be avoided. Wear appropriate protective equipment such as lab gloves, glasses and laboratory goggles during use.
Last Update：2024-04-10 22:29:15
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CAS: 87494-13-1
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CAS: 87494-13-1
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Email: 3008007409@qq.com
Mobile: 18021002903
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