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Detail of "5044-52-0"

  • CAS Number:
  • 5044-52-0
  • Name:

  • Phosphonium,ethenyltriphenyl-, bromide (1:1)

  • Superlist Name:
  • Triphenylvinylphosphonium bromide
  • Molecular Structure:
  • Formula:
  • C20H18P.Br
  • Molecular Weight:
  • 369.23
  • Synonyms:
  • Phosphonium,ethenyltriphenyl-, bromide (9CI);Phosphonium, triphenylvinyl-, bromide (8CI);Triphenylvinylphosphonium bromide (7CI);NSC 84065;Vinyltriphenylphosphoniumbromide;
  • EINECS:
  • 225-740-3
  • Melting Point:
  • 176-178 °C(lit.)
  • Appearance:
  • white to beige fine crystalline powder
  • Hazard Symbols:
  • IrritantXi
  • Risk Codes:
  • 36/37/38
  • Safety:
  • 22-24/25 Details
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CAS No.5044-52-0 Triphenylvinylphosphonium bromide

Supplier:Ruiyuan Group Limited [ China (Mainland)]

Platinum
Supplier 1555Integral
1555

Tel:+86 21 50456736

Address:No.188,Zhangyang Road,Shanghai

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CAS No.5044-52-0 Triphenylvinylphosphonium bromide

Supplier:Hangzhou Dayangchem Co., Ltd. [ China (Mainland)]

Platinum
SupplierISO 3875Integral
3875

Tel:+86-571-88938639

Address:B/2601 Fuli Building, 328# WenEr Rd. Hangzhou City 310012 China

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CAS No.5044-52-0 Triphenylvinylphosphonium bromide

98%

Supplier:Vscichem Technology (BeiJing) Co.,Ltd. [ China (Mainland)]

610Integral
610

Tel:010-60270130 13466675073，15110140565

Address:beijing,china

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CAS No.5044-52-0 Triphenylvinylphosphonium bromide

Supplier:Zhengzhou Alfachem Co., Ltd. [ China (Mainland)]

600Integral
600

Tel:0371-55616343

Address:zhengzhou

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CAS No.5044-52-0 Triphenylvinylphosphonium bromide

Supplier:AHH Chemical Co.,Ltd [ China (Mainland)]

600Integral
600

Tel:86-27-87598316

Address:B-720,Guanggu International Blg,456 LuoYu Rd,

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Reference

A synthesis of ibogamine
A synthesis of ibogamine. Kuehne, Martin E.; Reider, Paul J. 5044-52-0 are also occured in this study. (Dep. Chem., Univ. Vermont, Burlington, VT 05405, USA). There are some commonly used reagents like 5044-52-0 in this article. J. Org. Chem., 50(9), 1464-7 (English) 1985. CODEN: JOCEAH. ISSN: 0022-3263. DOCUMENT TYPE: Journal CA Section: 31 (Alkaloids) A synthesis of ibogamine (I) was developed by elaboration of 5-carbomethoxy-3-ethylcyclohexene. The latter was obtained as a 1:1 epimeric mixt. from condensation of di-Et (2-ethyl-1-oxo-3-propyl)malonate with triphenylvinylphosphonium bromide, followed by hydrolysis, decarboxylation and esterification. ..
A synthesis of ibogamine
A synthesis of ibogamine. Kuehne, Martin E.; Reider, Paul J. 5044-52-0 are also occured in this study. (Dep. Chem., Univ. Vermont, Burlington, VT 05405, USA). There are some commonly used reagents like 5044-52-0 in this article. J. Org. Chem., 50(9), 1464-7 (English) 1985. CODEN: JOCEAH. ISSN: 0022-3263. DOCUMENT TYPE: Journal CA Section: 31 (Alkaloids) A synthesis of ibogamine (I) was developed by elaboration of 5-carbomethoxy-3-ethylcyclohexene. The latter was obtained as a 1:1 epimeric mixt. from condensation of di-Et (2-ethyl-1-oxo-3-propyl)malonate with triphenylvinylphosphonium bromide, followed by hydrolysis, decarboxylation and esterification. ..
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