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149329-29-3

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149329-29-3 Usage

Uses

3-Chloro-1,1,1,3-tetrafluoropropane is a useful reagent for fluorination of chloropropenes.

Check Digit Verification of cas no

The CAS Registry Mumber 149329-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,3,2 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 149329-29:
(8*1)+(7*4)+(6*9)+(5*3)+(4*2)+(3*9)+(2*2)+(1*9)=153
153 % 10 = 3
So 149329-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C3H3ClF4/c4-2(5)1-3(6,7)8/h2H,1H2

149329-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-CHLORO-1,1,1,3-TETRAFLUOROPROPANE

1.2 Other means of identification

Product number -
Other names 1,1,1,3-tetrafluoro-3-chloropropane

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:149329-29-3 SDS

149329-29-3Relevant articles and documents

Process system and method for producing trans-1-chloro-3,3,3-trifluoropropene

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Paragraph 0034; 0057-0058, (2021/04/14)

The invention discloses a process system and method for producing trans-1-chloro-3,3,3-trifluoropropene. Hydrogen fluoride and 1,1,1,3,3-pentachloropropane are subjected to a liquid phase fluorination reaction in a liquid phase catalytic reactor, the trans-1-chloro-3,3,3-trifluoropropene is synthesized, and cis-1-chloro-3,3,3-trifluoropropene and 3-chloro-1,1,1,3,3-tetrafluoropropane are byproducts. In a gas-phase catalytic reactor, the byproducts cis-1,3,3,-trifluoropropene and 3-chloro-1,1,1,3-tetrafluoropropane react with HCl, and are further converted into the trans-1-chloro-3,3,3-trifluoropropene. By adopting the method, the trans-1-chloro-3,3,3-trifluoropropene can be produced with high yield, the optimal conversion of materials is realized, main by-products are circularly converted into target products, and the separation problem of approximate azeotrope HCFO-1233zd(Z) and HCFC-244fa is avoided.

INTEGRATED PROCESS FOR THE CO-PRODUCTION OF TRANS-1-CHLORO-3,3,3-TRIFLUOROPROPENE, TRANS-1,3,3,3-TETRAFLUOROPROPENE, AND 1,1,1,3,3-PENTAFLUOROPROPANE

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Paragraph 0077; 0078; 0079, (2013/10/08)

Disclosed is an integrated process to co-produce trans-1-chloro-3,3,3-trifluoro-propene (1233zd (E)), trans-1,3,3,3-tetrafluoropropene (1234ze (E)), and 1,1,1,3,3-pentafluoropropane (245fa). Overall the co-production is a three-step process. The chemistry involves the steps of: (1) the reaction of 1,1,1,3-tetrachloropropene and/or 1,1,3,3-tetrachloropropene with anhydrous HF in excess in a liquid-phase catalyzed reactor in such a way as to co-produce primarily 1233zd (E) and 244fa (plus by-product HCl); an optionally(2) the 244fa stream can then be used to directly produce any (or all) of the following desired products;(a) the 244fa stream can be dehydrochlorinated to produce the desired second product 1234ze (E); and/or(b) the 244fa stream can be dehydrofluorinated to produce 1233zd (E) if more of that product is desired; and/or(c) the 244fa stream can be further fluorinated to form 245fa.

INTEGRATED PROCESS TO CO-PRODUCE 1,1,1,3,3-PENTAFLUOROPROPANE, TRANS-1-CHLORO-3,3,3-TRIFLUOROPROPENE and TRANS-1,3,3,3-TETRAFLUOROPROPENE

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Page/Page column 6, (2012/11/07)

Disclosed is a fully integrated process for making 1,1,1,3,3-pentafluoropropane (HFC-245fa), trans-1-chloro-3,3,3-trifluoropropene (HCFO-1233zd(E)), and trans-1,3,3,3-tetrafluoropropene (HFO-1234ze(E)). The chemistry involves (a) the reaction of 1,1,1,3,3-pentachloropropane (HCC-240fa), or a derivative thereof selected from 1,1,3,3-tetrachloropropene and 1,3,3,3-tetrachloropropene, with anhydrous HF in excess in the presence of a catalyst in a liquid-phase reactor in such a way as to co-produce HCFO-1233zd, HFO-1234ze, HCFC-244fa (3-chloro-1,1,1,3-tetrafluoropropane), and HFC-245fa in a first reactor; (b) the reaction of HCFO-1233zd and HFO-1234ze with HCl in excess in the presence of a catalyst in a second reactor to convert these two olefins into HCFC-243fa and HCFC-244fa, respectively; (c) the reaction of HCFC-243fa and HCFC-244fa over a dehydrochlorination catalyst or in a caustic solution in a third reactor to form HCFO-1233zd and HFO-1234ze; and (d) the reaction of HCFO-1233zd(Z) and HFO-1234ze(Z) in the presence of a catalyst in a fourth reactor to form trans-1233zd and trans-1234ze, respectively.

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