N-(Trifluoroacetyl)glycine
- Product Name
- N-(Trifluoroacetyl)glycine
- CAS No.
- 383-70-0
- Chemical Name
- N-(Trifluoroacetyl)glycine
- Synonyms
- TFA-Gly;TFA-GLY-OH;TFA-GLYCINE;TRIFLUOROACETYL GLYCINE;n-(trifluoroacetyl)glycine;L- trifluoroacetyl glycine;glycine,N-(trifluoroacetyl)-;N-alpha-Trifluoracetyl-glycin;(2,2,2-trifluoroacetyl)glycine;N-ALPHA-TRIFLUOROACETYL-GLYCINE
- CBNumber
- CB0383547
- Molecular Formula
- C4H4F3NO3
- Formula Weight
- 171.07
- MOL File
- 383-70-0.mol
N-(Trifluoroacetyl)glycine Property
- Melting point:
- 120-121 °C
- Boiling point:
- 291.6°C
- Density
- 1.534
- Flash point:
- 130°C
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- Chloroform, DMSO
- form
- Solid
- pka
- 2.99±0.10(Predicted)
- color
- White
- InChI
- InChI=1S/C4H4F3NO3/c5-4(6,7)3(11)8-1-2(9)10/h1H2,(H,8,11)(H,9,10)
- InChIKey
- IFAXXCBMQJNCCF-UHFFFAOYSA-N
- SMILES
- C(O)(=O)CNC(C(F)(F)F)=O
- CAS DataBase Reference
- 383-70-0
- NIST Chemistry Reference
- N-(Trifluoroacetyl)aminoacetic acid(383-70-0)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P321Specific treatment (see … on this label).
P330Rinse mouth.
P332+P313IF SKIN irritation occurs: Get medical advice/attention.
P362Take off contaminated clothing and wash before reuse.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- T787205
- Product name
- N-Trifluoroacetylglycine
- Packaging
- 10g
- Price
- $415
- Updated
- 2021/12/16
- Product number
- T8416-28
- Product name
- N-Trifluoroacetylglycine
- Packaging
- 500mg
- Price
- $355
- Updated
- 2021/12/16
- Product number
- 099637
- Product name
- 2-(2,2,2-Trifluoroacetamido)acetic acid
- Purity
- 95+%
- Packaging
- 10g
- Price
- $395
- Updated
- 2021/12/16
- Product number
- AAA0002018
- Product name
- N-TRIFLUOROACETYLGLYCINE
- Purity
- 95.00%
- Packaging
- 5G
- Price
- $1114.58
- Updated
- 2021/12/16
- Product number
- 13982
- Product name
- N-Trifluoroacetylglycine
- Packaging
- 2.5g
- Price
- $1880
- Updated
- 2021/12/16
N-(Trifluoroacetyl)glycine Chemical Properties,Usage,Production
Chemical Properties
White Solid
Uses
N-Trifluoroacetylglycine (cas# 383-70-0) is a compound useful in organic synthesis.
Definition
ChEBI: N-(trifluoroacetyl)glycine is an N-acylglycine resulting from the formal condensation of the amino group of glycine with the carboxy group of trifluoroacetic acid. It is a N-acylglycine, a secondary carboxamide and a trifluoroacetamide.
Synthesis
383-63-1
56-40-6
383-70-0
The general procedure for the synthesis of 2-(2,2,2-trifluoroacetamido)acetic acid from ethyl trifluoroacetate and glycine was carried out as follows: the TFA-α-amino acid was prepared by the method reported in references [1,2] with slight modifications. First, triethylamine (33 mmol, 1.5 eq.) was added to a methanolic solution (22 mL) of glycine (22 mmol). after 5 min, ethyl trifluoroacetate (29 mmol, 1.3 eq.) was added and the reaction mixture was stirred for 24 h. The reaction was carried out by rotary evaporation. Upon completion of the reaction, the solvent was removed by rotary evaporation. The remaining residue was dissolved in water (35 mL) and acidified with concentrated hydrochloric acid (4 mL). After acidification, the mixture was stirred for 15 minutes and then extracted with ethyl acetate. The organic layers were combined, washed sequentially with water and brine, and dried with anhydrous magnesium sulfate. After drying, filter and concentrate by rotary evaporation. If cured products (e.g., L-1a, D-1a, L-2a, D-2a, 3a, L-4a, D-4a to D-8a) are desired, they can be further dried overnight under high vacuum.
References
[1] Organic and Biomolecular Chemistry, 2015, vol. 13, # 30, p. 8298 - 8309
[2] Organic Letters, 2018, vol. 20, # 18, p. 5877 - 5880
[3] Molecules, 2017, vol. 22, # 10,
[4] European Journal of Organic Chemistry, 2012, # 29, p. 5774 - 5788,15
[5] European Journal of Organic Chemistry, 2012, # 29, p. 5774 - 5788
N-(Trifluoroacetyl)glycine Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from N-(Trifluoroacetyl)glycine manufacturers
- Product
- N-(Trifluoroacetyl)glycine 383-70-0
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 20t
- Release date
- 2024-06-25
- Product
- N-(Trifluoroacetyl)glycine 383-70-0
- Price
- US $0.00/KG
- Min. Order
- 1KG
- Purity
- 98.9%
- Supply Ability
- 100 tons
- Release date
- 2022-02-21