170899-08-8
(R)-N-BOC-Allylglycine
CAS: 170899-08-8
Molecular Formula: C10H17NO4
170899-08-8 - Names and Identifiers
| Name | (R)-N-BOC-Allylglycine |
| Synonyms | Boc-D-Allylglycine RARECHEM BK PT 0253 BOC-ALPHA-ALLYL-D-GLY Boc-D-Allyglycine·DCHA Boc-(R)-2-Allylglycine (R)-N-BOC-Allylglycine (R)-N-BOC-ALLYLGLYCINE Boc-D-Allylglycine.DCHA (R)-N-boc-Allylglycine(e.e.) BOC-(R)-2-AMINO-4-PENTENOIC ACID (2R)-2-[(tert-butoxycarbonyl)amino]pent-4-enoate (R)-N-tert-Butoxycarbonyl-2-amino-4-pentenoic acid (R)-N-TERT-BUTOXYCARBONYL-2-AMINO-4-PENTENOIC ACID |
| CAS | 170899-08-8 |
| InChI | InChI=1/C12H23N.C10H17NO4/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;1-5-6-7(8(12)13)11-9(14)15-10(2,3)4/h11-13H,1-10H2;5,7H,1,6H2,2-4H3,(H,11,14)(H,12,13)/t;7-/m.1/s1 |
170899-08-8 - Physico-chemical Properties
| Molecular Formula | C10H17NO4 |
| Molar Mass | 215.25 |
| Density | 1.1835 (rough estimate) |
| Boling Point | 355.52°C (rough estimate) |
| Flash Point | 283.8°C |
| Vapor Presure | 2.38E-13mmHg at 25°C |
| Appearance | Viscous Liquid Clear pale yellow |
| Color | Clear pale yellow |
| pKa | 3.83±0.10(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.4610 (estimate) |
170899-08-8 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| HS Code | 29224985 |
| Hazard Class | IRRITANT |
170899-08-8 - Upstream Downstream Industry
170899-08-8 - Introduction
(R)-N-BOC-Allylglycine is an organic compound with the chemical formula C14H21NO5. It is a chiral amino acid with a protecting group Boc(tert-butyloxycarbonyl) and an allyl function. It is a derivative of D-glycine, obtained by introducing a Boc protecting group and an allyl function on its α-amino group.
(R)-N-BOC-Allylglycine are commonly used in biochemistry, organic synthesis, and pharmaceutical research. Because it is a chiral molecule, it can be used to synthesize chiral compounds and drugs. In addition, due to the activity and diversity of allyl functional groups,(R)-N-BOC-Allylglycine can also be used as synthetic intermediates to participate in more complex organic synthesis reactions for the construction of complex chemical structures.
Preparation of (R)-N-BOC-Allylglycine are generally chemically synthesized. A common preparation method is to use D-glycine and Boc-allyl alcohol for esterification, and then remove the protecting Group of the product, and finally obtain (R)-N-BOC-Allylglycine.
Regarding safety information,(R)-N-BOC-Allylglycine are chemical reagents, and attention should be paid to safe operation during use. It may be irritating to the eyes, skin and respiratory tract, so use protective glasses, gloves and a mask. In addition, the laboratory's chemical storage and handling practices should be followed to avoid contact with ignition sources or reactions with other chemicals. It should be kept separate from other chemicals for use and storage. For detailed safety information, please refer to the relevant chemical Safety Data Sheet (MSDS). To ensure safety, please use and handle the compound under the guidance of professionals.
(R)-N-BOC-Allylglycine are commonly used in biochemistry, organic synthesis, and pharmaceutical research. Because it is a chiral molecule, it can be used to synthesize chiral compounds and drugs. In addition, due to the activity and diversity of allyl functional groups,(R)-N-BOC-Allylglycine can also be used as synthetic intermediates to participate in more complex organic synthesis reactions for the construction of complex chemical structures.
Preparation of (R)-N-BOC-Allylglycine are generally chemically synthesized. A common preparation method is to use D-glycine and Boc-allyl alcohol for esterification, and then remove the protecting Group of the product, and finally obtain (R)-N-BOC-Allylglycine.
Regarding safety information,(R)-N-BOC-Allylglycine are chemical reagents, and attention should be paid to safe operation during use. It may be irritating to the eyes, skin and respiratory tract, so use protective glasses, gloves and a mask. In addition, the laboratory's chemical storage and handling practices should be followed to avoid contact with ignition sources or reactions with other chemicals. It should be kept separate from other chemicals for use and storage. For detailed safety information, please refer to the relevant chemical Safety Data Sheet (MSDS). To ensure safety, please use and handle the compound under the guidance of professionals.
Last Update：2024-04-09 21:04:16
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CAS: 170899-08-8
Tel: +86 0512-68417696
Email: linda@highfine.com
minhan.zhao@highfine.com
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Spot supply
Product Name: Boc-D-Allylglycine Visit Supplier Webpage Request for quotationCAS: 170899-08-8
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922
Wechat: 18621343501
WhatsApp: +86-18621343501
Product Name: (S)-2-(tert-butoxycarbonyl)pent-4-enoic acid Request for quotation
CAS: 170899-08-8
Tel: +86 0512-68417696
Email: linda@highfine.com
minhan.zhao@highfine.com
QQ: 4006286883
CAS: 170899-08-8
Tel: +86 0512-68417696
Email: linda@highfine.com
minhan.zhao@highfine.com
QQ: 4006286883
View History
170899-08-8
4-phenylmorpholin-3-one
Galanthamine
TERT
12-DEOXYPHORBOL 13-ANGELATE 20-ACETATE
176504-01-1
Z-ARG-ARG-MCA(HYDROCHLORIDE FORM)
Valsartan-d9
N-(2,6-dimethylphenyl)nicotinamide
ETHYL 2-CHLORO-2-[2-(2-FLUOROPHENYL)HYDRAZONO]-ACETATE
4-phenylmorpholin-3-one
Galanthamine
TERT
12-DEOXYPHORBOL 13-ANGELATE 20-ACETATE
176504-01-1
Z-ARG-ARG-MCA(HYDROCHLORIDE FORM)
Valsartan-d9
N-(2,6-dimethylphenyl)nicotinamide
ETHYL 2-CHLORO-2-[2-(2-FLUOROPHENYL)HYDRAZONO]-ACETATE
Raw Materials for 170899-08-8