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D-2-Amino-1,1,1-Trifluoro-3-(Methyl)Butane is a chemical compound that features an amino group, a trifluoro functional group, and a butane backbone. It is also known by systematic names such as 2-Amino-1,1,1-trifluoro-3-methylbutane and (2S)-2-amino-3-methyl-1,1,1-trifluorobutane. The presence of methyl and butane groups indicates its organic nature, while the trifluoro component highlights the inclusion of three fluorine atoms in its molecular structure. The exact chemical and physical properties or potential applications of D-2-AMINO-1,1,1-TRIFLUORO-3-(METHYL)BUTANE are currently unspecified.

1582-18-9

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1582-18-9 Usage

Uses

Since the provided materials do not specify the exact applications of D-2-Amino-1,1,1-Trifluoro-3-(Methyl)Butane, it is not possible to list its uses based on the information given. However, given its chemical structure, it may have potential applications in various industries such as pharmaceuticals, chemical manufacturing, or materials science, depending on its properties and reactivity. Further research and experimentation would be required to determine its specific uses and benefits in these or other fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1582-18-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,8 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1582-18:
(6*1)+(5*5)+(4*8)+(3*2)+(2*1)+(1*8)=79
79 % 10 = 9
So 1582-18-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H10F3N/c1-3(2)4(9)5(6,7)8/h3-4H,9H2,1-2H3/t4-/m1/s1

1582-18-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name DL-2-Amino-1,1,1-trifluoro-3-methylbutane

1.2 Other means of identification

Product number -
Other names DL-2-Amino-1,1,1-trifluoro-3-methylbutane hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1582-18-9 SDS

1582-18-9Downstream Products

1582-18-9Relevant academic research and scientific papers

Economical and practical strategies for synthesis of α-trifluoromethylated amines

Jiang,Cheng,Yuan

, p. 2406 - 2408 (2016/05/19)

A powerful approach to synthesize α-trifluoromethylated amines has been developed. The method is operationally simple, broad in substrate scope and amenable to scale-up using trifluoroacetic anhydride. Meanwhile, the strategy not only provided a versatile approach to synthesize α-trifluoromethylated amines but also provides a new method for exploring the new reactivity of trifluoroacetic anhydride.

Chemoenzymatic dynamic kinetic resolution of α-trifluoromethylated amines: Influence of substitutions on the reversed stereoselectivity

Cheng, Guilin,Xia, Bo,Wu, Qi,Lin, Xianfu

, p. 9820 - 9828 (2013/09/02)

Enzymatic resolution of α-trifluoromethylated amines via kinetic resolution (KR), dynamic kinetic resolution (DKR) employing CALB-Pd/Al 2O3, and a one-pot sequential process of KR/DKR/KR was investigated comparatively for the first time. Although CALB-catalyzed KR of α-trifluoromethylated amines with substituents of methyl (1a), isopropyl (1c), phenyl (1d) and benzyl group (1e) can provide good stereoselectivity factors E from 31 to >200 respectively, DKR and sequential process of KR/DKR/KR possess better practical application potential because of the higher conversion (62%-84%) and the similar enantiomeric excesses (90%-99%). The enantiopreference and inversion for the α-trifluoromethylated amines displayed by CALB were observed and explained by docking modes. Namely, for 1,1,1-trifluoro-2-propylamine (1a), the product amide with R-configuration was obtained, and the enantiopreference was converted to S for the amines (1b-1e) with substituents larger than methyl group. The catalysts recycle, and scale-up experiments were demonstrated successfully. All these results indicated the high efficiency and green feature of this enzymatic process, and its application significance.

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