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121899-81-8

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121899-81-8 Usage

General Description

DICHLOROTRIS(2-METHOXYPHENYL)BISMUTH is a chemical compound that is characterized by the presence of three 2-methoxyphenyl groups attached to a central bismuth atom, with each phenyl group being coordinated to the bismuth atom through a dichloro ligand. DICHLOROTRIS(2-METHOXYPHENYL)BISMUTH is often used as a reagent in organic synthesis reactions and can also be utilized in catalytic processes. Additionally, it has been investigated for its potential antimicrobial and antitumor properties. DICHLOROTRIS(2-METHOXYPHENYL)BISMUTH is a relatively stable and non-toxic compound, making it suitable for various applications in chemical research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 121899-81-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,8,9 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 121899-81:
(8*1)+(7*2)+(6*1)+(5*8)+(4*9)+(3*9)+(2*8)+(1*1)=148
148 % 10 = 8
So 121899-81-8 is a valid CAS Registry Number.
InChI:InChI=1/3C7H7O.Bi.2ClH/c3*1-8-7-5-3-2-4-6-7;;;/h3*2-5H,1H3;;2*1H/q;;;+2;;/p-2/rC21H21BiCl2O3/c1-25-19-13-7-4-10-16(19)22(23,24,17-11-5-8-14-20(17)26-2)18-12-6-9-15-21(18)27-3/h4-15H,1-3H3

121899-81-8 Well-known Company Product Price

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  • TCI America

  • (T1956)  Tris(2-methoxyphenyl)bismuth Dichloride  >98.0%(T)

  • 121899-81-8

  • 1g

  • 990.00CNY

  • Detail
  • TCI America

  • (T1956)  Tris(2-methoxyphenyl)bismuth Dichloride  >98.0%(T)

  • 121899-81-8

  • 5g

  • 3,450.00CNY

  • Detail

121899-81-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Dichlorotris(2-methoxyphenyl)bismuth

1.2 Other means of identification

Product number -
Other names dichloro-tris(2-methoxyphenyl)bismuth

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:121899-81-8 SDS

121899-81-8Relevant articles and documents

HERBICIDE COMPOSITION

-

, (2015/11/03)

There is provided a herbicidal composition containing a cyclohexanone compound represented by Formula (I) and at least one compound selected from Group A. Group A: consisting of benoxacor, cloquintocet-mexyl, cyometrinil, dichlormid, fenchlorazole-ethyl,

Unexpected formation of highly stabilized tetrakis-(2-alkoxyphenyl)bismuthonium salts in the oxidation of tris-(2-alkoxyphenyl)bismuthanes with iodosylbenzene

Suzuki, Hitomi,Ikegami, Tohru,Azuma, Nagao

, p. 1609 - 1616 (2007/10/03)

Treatment of tris-(2-alkoxyphenyl)bismuthanes 1 with iodosylbenzene in methylene dichloride at 40°C led to none of the expected bismuthane oxides 2 but, quite unexpectedly, gave tetrakis-(2-alkoxyphenyl)bismuthonium chlorides 3 in moderate to good yields. In some cases, bismuthonium formates 4 accompanied the main reaction products. Similar treatment in benzene in the presence of benzyl bromide, ethyl bromide, or 2,2,2-trifluoroethyl iodide led to the corresponding bismuthonium bromides 7 and iodides 8. Through anion exchange, a variety of bismuthonium salts including formate 4, tetrafluoroborate 11, toluene-p-sulfonate 12, bromide 7, iodide 8 and perchlorate 13 were prepared from the salt 3 in good yields. In contrast to the known tetraphenylbismuthonium salts, all of these new bismuthonium salts exhibited high thermal stability. The molecular structure of compound 7a was elucidated by X-ray analysis, where the four neighbouring oxygen atoms are found to surround the bismuth atom tetrahedrally via a weak through-space interaction with the metal, making the bismuth centre less susceptible to nucleophilic attack of the halide anion.

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