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67230-92-6

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67230-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67230-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,3 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67230-92:
(7*6)+(6*7)+(5*2)+(4*3)+(3*0)+(2*9)+(1*2)=126
126 % 10 = 6
So 67230-92-6 is a valid CAS Registry Number.

67230-92-6Relevant articles and documents

Reaction of halothane with carbonyl compounds in the presence of bases

Ando, Akira,Takahashi, Junko,Nakamura, Yuki,Maruyama, Naoki,Nishihara, Masakazu,Fukushima, Kaori,Moronaga, Jin,Inoue, Mayumi,Sato, Kazuyuki,Omote, Masaaki,Kumadaki, Itsumaro

, p. 283 - 285 (2007/10/03)

The reaction of halothane, 2-bromo-2-chloro-1,1,1-trifluoroethane (1), with aldehydes and ketones in the presence of bases was found to give 1-alkyl- or 1-aryl-2-bromo-2-chloro-3,3, 3-trifluoropropanols (2) or 2-chloro-3,3-difluoro-2-propenols (3) selecti

Synthesis of fluorine compounds using zinc complex of halothane

Takagi, Toshiyuki,Nakamoto, Makoto,Sato, Kazuyuki,Koyama, Mayumi,Ando, Akira,Kumadaki, Itsumaro

, p. 12667 - 12676 (2007/10/03)

We have reported the Grignard reaction of Halothane, 2-bromo-2-chloro-1,1,1-trifluoroethane (1), with ketones gave unexpected products, α-(1-bromo-1-chloro-2,2,2-trifluoroethyl)alcohols (4) at a low temperature. However, this reaction hardly proceeded with aldehydes. Now, we found the reaction of 1 with aldehydes in the presence of zinc gave not only products of type 4, but α-(1-chloro-2,2,2-trifluoroethyl)alcohols (3), the expected type of products, under mild conditions in good to moderate yields.

Synthetic utility of HCFC-123 (2,2-dichloro-1,1,1-trifluoroethane): the reaction between HCFC-123 and aldehydes using zinc

Tamura, Masanori,Sekiya, Akira

, p. 119 - 122 (2007/10/02)

HCFC-123 (2,2-dichloro-1,1,1-trifluoroethane) reacted with zinc and aldehydes to afford predominantly either 1-substituted 2-chloro-3,3-difluoro-2-propen-1-ols or 1-substituted 2,2-dichloro-3,3,3-trifluoro-1-propanols.The reactions proceeded via 1,1-dichloro-2,2,2-trifluoroethylzinc chloride as an organozinc intermediate. - Keywords: 2,2-Dichloro-1,1,1-trifluoroethane; Reaction; Aldehydes; Zinc; 1,1-Dichloro-2,2,2-trifluoroethylzinc chloride

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