Name: | (CARBOMETHOXYMETHYL)TRIPHENYLPHOSPHONIUM BROMIDE |
CAS: | 1779-58-4 |
Synonyms: | CMMTPPB ; (METHOXYCARBONYLMETHYL)TRIPHENYLPHOSPHONIUM BROMIDE, 98+% ; PHOSPHONIUM, (2-METHOXY-2-OXOETHYL)TRIPHENYL-, BROMIDE ; (2-METHOXY-2-OXOETHYL)TRIPHENYLPHOSPHONIUM BROMIDE ; CARBMETHOXY METHYL TRIPHENYL PHOSPHONIUM BROMIDE ; METHOXYCARBONYLMETHYTLTRIPHENYLPHOSPHONIUMBROMIDE ; (CARBOMETHOXYMETHYL)TRIPHENYLPHOSPHONIUM BROMIDE ; METHYL (TRIPHENYLPHOSPHONIO)ACETATE BROMIDE ; (METHOXYCARBONYLMETHYL)TRIPHENYLPHOSPHONIUM BROMIDE |
MDL.: | MFCD00011801 |
H bond acceptor: | 2 |
H bond donor: | 0 |
Smile: | COC(=O)C[P+](c1ccccc1)(c2ccccc2)c3ccccc3.[Br-] |
InChi: | InChI=1S/C21H20O2P.BrH/c1-23-21(22)17-24(18-11-5-2-6-12-18,19-13-7-3-8-14-19)20-15-9-4-10-16-20;/h2-16H,17H2,1H3;1H/q+1;/p-1 |
InChiKey: | InChIKey=VCWBQLMDSMSVRL-UHFFFAOYSA-M |
Property |
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Melting Point: | 165-170 DEG C (DEC)(LIT) |
Comments: | APPLICATION: REACTANT FOR SYNTHESIS OF: GSK-3 INHIBITORS USING THEWITTIG REACTION. SUBSTITUTED FURANONES FOR ANTIFUNGAL AND CYTOSTATIC ACTIVITIES. PHOTOCHROMIC DITHIENYLETHENE DERIVATIVES. GEM-DIIODOALKANES CONTAINING ALLYLIC ALCOHOLS. HIGHLY SUBSTITUTED CYCLOPENTENES AND BRAZILANES VIA AU-CATALYZED DEOXYGENATIVE NAZAROV CYCLIZATION. REACTANT FOR: ASYMMETRIC HYDROGENATION OF ALPHA,BETA-UNSATURATED ESTER-PHOSPHONATES. STUDIES OF THERMAL DECOMPOSITION OF PHOSPHONIUM ALKYL ESTER SALTS NSC 136109 UNSPSC: 12352103 WGK: 3 |
Safety information |
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Symbol: |
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Signal word: | Warning |
Hazard statements: | H315-H319-H335 |
Precautionary statements: | P261-P305 + P351 + P338 |
hazard symbol: | Xi |
Risk Code: | R:36/37/38 |
Safe Code: | S:26-36 |
WGK Germany: | 3 |
(CARBOMETHOXYMETHYL)TRIPHENYLPHOSPHONIUM BROMIDE
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