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16500-91-7

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16500-91-7 Usage

Physical state

Colorless liquid It is a liquid without any color, which indicates its relatively low volatility and boiling point.

Odor

Faint, sweet The compound has a mild and sweet smell, which may not be easily detectable at low concentrations.

Primary use

Intermediate for the synthesis of other chemicals It is mainly used in the production of other chemical compounds, particularly pesticides and plastics.

Hazardous substance

Yes 1-Propene, 2,3,3,3-tetrachlorois considered hazardous due to its potential health and environmental risks.

Health effects

Skin, eye, and respiratory tract irritation Exposure to high levels of this compound can cause discomfort and irritation in these body parts.

Carcinogenic potential

Yes It has been classified as a potential carcinogen, which means it may cause cancer with prolonged or high-level exposure.

Environmental impact

Harmful if released into air or water The compound can have negative effects on the environment if it is not handled and stored properly.

Handling and storage precautions

Handle and store with caution To minimize potential risks to human health and the environment, it is important to follow proper safety procedures when working with 1-Propene, 2,3,3,3-tetrachloro-.

Check Digit Verification of cas no

The CAS Registry Mumber 16500-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,0 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16500-91:
(7*1)+(6*6)+(5*5)+(4*0)+(3*0)+(2*9)+(1*1)=87
87 % 10 = 7
So 16500-91-7 is a valid CAS Registry Number.

16500-91-7Relevant articles and documents

PROCESSES FOR PREPARING PENTACHLOROPROPANE AND TETRACHLOROPROPENE FROM DICHLOROPROPENE

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Paragraph 0092, (2022/04/03)

A processes for preparing 1,1,2,3-tetrachloropropene, 2,3,3,3-tetrachloropropene, or a mixture thereof from 1,3-dichloropropene. The process may include a two successive chlorination and dehydrochlorination reactions. In a first chlorination reaction 1,3-dichloropropene is reacted with a chlorination agent to form a first chlorination reaction product including 1,1,2,3-tetrachloropropane. This first chlorination reaction product is reacted with a dehydrochlorination reagent in a first dehydrochlorination reaction to form a first dehydrochlorination reaction product including a trichloropropene. The trichloropropene containing reaction product is reacted with a chlorination agent in a second chlorination reaction to form a second chlorination reaction product including at least one of 1,1,1,2,3-pentachloropropane or 1,1,2,2,3-pentachloropropane. This reaction product is reacted with a dehydrochlorination reagent in a second dehydrochlorination reaction to form a second dehydrochlorination reaction product having 1,1,2,3-tetrachloropropene or a 2,3,3,3-tetrachloropropene.

PROCESS FOR THE PRODUCTION OF CHLORINATED PROPANES AND/OR PROPENES

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Paragraph 0078-0082, (2013/06/05)

Processes for the production of chlorinated propanes and/or propenes are provided. The present processes make use of methylacetylene, a by-product in the production of ethylene and/or propylene, as a low cost starting material, alone or in combination with propadiene, propene and/or propane. In the latter embodiments, the processes may also be utilized to provide a substantially pure stream of propane.

PROCESS FOR PREPARING 2-CHLORO-3,3,3-TRIFLUOROPROPENE

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Page/Page column 11; 12, (2010/11/05)

The present invention provides a process for preparing 2-chloro-3,3,3-trifluoropropene including subjecting, in the absence of a catalyst, at least one chlorine-containing compound selected from the group consisting of chloropropane represented by formula (1): CClX2CHClCH2Cl, wherein each X is the same or different and each represents Cl or F, chloropropene represented by formula (2): CClY2CCl=CH2, wherein each Y is the same or different and each represents Cl or F, and chloropropene represented by formula (3): CZ2=CClCH2Cl, wherein each Z is the same or different and each represents Cl or F, to a reaction with hydrogen fluoride under heating in a gas phase. According to the present invention, 2-chloro-3,3,3-trifluoropropene (HCFC-1233xf) can be effectively prepared by an easy and economically advantageous process that is suitable for industrial scale production.

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