추천 제품
분석
95%
형태
liquid
refractive index
n20/D 1.532 (lit.)
density
1.116 g/mL at 25 °C (lit.)
SMILES string
CCCC[Sn](CCCC)(CCCC)C#Cc1ccccc1
InChI
1S/C8H5.3C4H9.Sn/c1-2-8-6-4-3-5-7-8;3*1-3-4-2;/h3-7H;3*1,3-4H2,2H3;
InChI key
PYMPTRMDPJYTDF-UHFFFAOYSA-N
애플리케이션
Tributyl(phenylethynyl)tin can be used:
- As a substrate in the palladium-catalyzed homocoupling of organostannanes to yield biaryl compounds.
- To prepare various enynals, which are employed in the synthesis of substituted benzene derivatives catalyzed by nickel.
- In one of the key synthetic steps for the preparation of β-alkynylcorroles.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Repr. 1B - Skin Irrit. 2 - STOT RE 1
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point (°F)
235.4 °F - closed cup
Flash Point (°C)
113 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Efficient Synthesis of beta-Alkynylcorroles
European Journal of Organic Chemistry, 2015(31), 6811-6816 (2015)
Palladium-iminophosphine-catalyzed homocoupling of alkynylstannanes and other organostannanes using allyl acetate or air as an oxidant
Journal of Organometallic Chemistry, 670(1-2), 132-136 (2003)
A multicomponent approach to substituted benzenes involving sequential nickel-catalyzed reactions
Tetrahedron, 62(49), 11460-11469 (2006)
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