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3-Hydroxy-4,4,4-trichlorobutyric beta-lactone is a chemical compound with the molecular formula C4H5Cl3O3. It is a white crystalline solid that is soluble in water and various organic solvents. 3-hydroxy-4,4,4-trichlorobutyric beta-lactone is known for its potential use as a herbicide, specifically targeting the growth of certain plants by inhibiting their photosynthetic processes. It is characterized by its unique structure, which includes a beta-lactone ring and a hydroxyl group, along with three chlorine atoms attached to the butyric acid backbone. Due to its chemical properties and potential applications, 3-hydroxy-4,4,4-trichlorobutyric beta-lactone is a subject of interest in the field of agrochemicals and environmental science.

5895-35-2

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5895-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5895-35-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,9 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5895-35:
(6*5)+(5*8)+(4*9)+(3*5)+(2*3)+(1*5)=132
132 % 10 = 2
So 5895-35-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H3Cl3O2/c5-4(6,7)2-1-3(8)9-2/h2H,1H2

5895-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(trichloromethyl)oxetan-2-one

1.2 Other means of identification

Product number -
Other names 3-(Trichlormethyl)propan-3-olid

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:5895-35-2 SDS

5895-35-2Relevant academic research and scientific papers

Total Synthesis of Biselide A, A Cytotoxic Macrolide of Marine Origin

Hayakawa, Ichiro,Okamura, Masami,Suzuki, Kazuaki,Shimanuki, Mami,Kimura, Kizuku,Yamada, Takuya,Ohyoshi, Takayuki,Kigoshi, Hideo

, p. 2958 - 2970 (2017/06/27)

The total synthesis of biselide A based on our earlier strategy of synthesizing haterumalides is reported. The highlights of this approach are the use of regioselective enzymatic hydrolysis for the installation of a C20 oxygen functional group and an asymmetric aldol reaction for the stereoselective introduction of a C3 oxygen functional group.

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