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| | 1,4-Phenylenebis[tributylstannane] Basic information |
| Product Name: | 1,4-Phenylenebis[tributylstannane] | | Synonyms: | 1,4-Bis(tributylstannanyl)benzene;1,4-Bis(tributylstannyl)benzene;1,4-Phenylenebis[tributylstannane];Phenylene-1,4-bis(tributylstannane), Benzene-1,4-diylbis(tributylstannane);tributyl-(4-tributylstannylphenyl)stannane;Stannane, 1,1'-(1,4-phenylene)bis[1,1,1-tributyl-;SKL1098;ributyl-(4-tributylstannylphenyl)stannane | | CAS: | 17151-51-8 | | MF: | C30H58Sn2 | | MW: | 656.2 | | EINECS: | | | Product Categories: | Chemical Synthesis;Organometallic Reagents;Organotin;Organotins | | Mol File: | 17151-51-8.mol | ![1,4-Phenylenebis[tributylstannane] Structure](CAS/GIF/17151-51-8.gif) |
| | 1,4-Phenylenebis[tributylstannane] Chemical Properties |
| Boiling point | 206-210 °C(Press: 0.04 Torr) | | density | 1.147g/mLat 25℃ | | refractive index | n20/D 1.522 | | Fp | >110°C | | form | liquid | | color | Clear |
| | 1,4-Phenylenebis[tributylstannane] Usage And Synthesis |
| Uses | Reactant for:• ;Preparation of covalent analogs of DNA base pairs and triplets from 9-benzyl-6-chloropurine via a Stille cross-coupling reaction1• ;Reaction with glucuronolactone derivatives in preparation of 3-C-iodomethyl, 6-C-iodomethyl and 6-C-iodophenyl derivatives as higher iodinated analogs of D-glucose2 | | Uses | Reactant for:
- Preparation of covalent analogs of DNA base pairs and triplets from 9-benzyl-6-chloropurine via a Stille cross-coupling reaction
- Reaction with glucuronolactone derivatives in preparation of 3-C-iodomethyl, 6-C-iodomethyl and 6-C-iodophenyl derivatives as higher iodinated analogs of D-glucose
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| | 1,4-Phenylenebis[tributylstannane] Preparation Products And Raw materials |
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