| Chemical Name | 2-Bromothiazole |
| CAS Number | 3034-53-5 |
| Alfabeta Name | BROMOTHIAZOLE 2- |
| MDL Number | MFCD00005316 |
| Synonym |
2-Bromothiazole
{LY} 2-Bromothiazole
{} {LY} 2-Bromothiazole
{} {} {LY} 2-Bromothiazole
{} {} {} {LY} 2-Bromothiazole
{} {} {} {} {LY} 2-Bromothiazole
{} {} {} {} {} {LY} 2-Bromothiazole
{} {} {} {} {} {} {LY} 2-Bromothiazole
{} {} {} {} {} {} {} {LY} 2-Bromothiazole
{} {} {} {} {} {} {} {} {LY} 2-Bromothiazole
{} {} {} {} {} {} {} {} {} {LY} 2-Bromothiazole
{} {} {} {} {} {} {} {} {} {} {LY} 2-Bromothiazole
{} {} {} {} {} {} {} {} {} {} {} {LY} 2-Bromothiazole
{} {} {} {} {} {} {} {} {} {} {} {} {LY} 2-Bromothiazole
{} {} {} {} {} {} {} {} {} {} {} {} {} {LY} 2-Bromothiazole
{} {} {} {} {} {} {} {} {} {} {} {} {} {}
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} 2-Bromothiazole
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {}
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} 2-Bromothiazole
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} 2-Bromothiazole
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {}
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {L |
| EC Number | 221-229-4 |
| Beilstein Registry Number | 105724 |
| PubChem Substance ID | 76430 |
| Chemical Name Translation | 2-溴噻唑 |
| Reaxys-RN | 105724 |
| InChIKey | RXNZFHIEDZEUQM-UHFFFAOYSA-N |
| LabNetwork Molecule ID | LN00004618 |
| InChI | InChI=1S/C3H2BrNS/c4-3-5-1-2-6-3/h1-2H |
| Canonical SMILES | BrC1=NC=CS1 |
| Warnings |
IRRITANT, FLAMMABLE |
| Signal word |
Warning |
GHS Symbol
| WGK Germany | 3 |
| Safety Statements | |
- S23 Do not breathe gas/fumes/vapour/spray (appropriate wording to be specified by the manufacturer) 不要吸入气体/烟雾/蒸汽/喷雾;
- S24/25 Avoid contact with skin and eyes 避免皮肤和眼睛接触;
|
| Risk Statements | |
- R36/37/38 Irritating to eyes, respiratory system and skin 对眼睛、呼吸系统和皮肤有刺激性
|
| Precautionary statements | |
- P280 Wear protective gloves/protective clothing/eye protection/face protection. 戴防护手套/防护服/眼睛的保护物/面部保护物。
- P501 Dispose of contents/container to..… 处理内容物/容器.....
- P261 Avoid breathing dust/fume/gas/mist/vapours/spray. 避免吸入粉尘/烟/气体/烟雾/蒸汽/喷雾。
- P305+P351+P338
- P210 Keep away from heat/sparks/open flames/hot surfaces. — No smoking. 远离热源/火花/明火/热的表面。——禁止吸烟。
- P403+P235
|
| Personal Protective Equipment |
Eyeshields, Gloves, half-mask respirator (US), multi-purpose combination respirator cartridge (US)
Eyeshields, Gloves, half-mask respirator (EU), half-mask respirator (US), multi-purpose combination respirator cartridge (US) |
| Storage condition |
-20°C
{LY} -20°C
2-8°C
<0°C
<;0
{} {LY} -20°C
{} {} {LY} -20°C
{} {} {} {LY} -20°C
{} {} {} {} {LY} -20°C
{} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} -20°C
{} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} |
| Hazard statements | |
- H227 Combustible liquid 可燃液体
|
| Hazard Codes |
Xi,F |
| UN Number |
1993 |
用于 5- 和 7-氮杂吲哚 N-芳基化反应的芳基卤化物。参与铜催化的氰化反应生成 2-氰基噻唑.
{ALF} 2-Lithiothiazole can be obtained by direct lithiation of thiazole or, more conveniently, by exchange with 2-bromothiazole using n-BuLi: J. Org. Chem., 53, 1748 (1988). It behaves as a valuable formyl anion equivalent, and as such has been applied, mainly by Dondoni's group, in the syntheses of a variety of products; see, e.g.: Tetrahedron Lett., 34, 7319, 7323, 7327 (1993). See also 2-(Trimethyl­silyl)­thiazole, B21903. Reaction of 2-lithiothiazole with nitrones gives ɑ-aminoaldehydes: Tetrahedron Lett., 33, 4221 (1992); stereocontrolled addition to C-galacto-pyranosylnitrone has been used in syntheses of destomic acid, a component of the antibiotics destomycin and hygromycin, and of lincosamine, the sugar component of the anticancer antibiotic lincomycin: Synlett, 78 (1993). For applications of 2-lithiothiazole in the synthesis of the aza-sugar (+)-galactostsin, see: J. Org. Chem., 60, 4749 (1995). The Thiazole Aldehyde Synthesis has been reviewed by Dondoni: Synthesis, 1681 (1998).
{TRC} Voogd, C.E., et al.: Mutation Research, Genetic Toxicology Testing, 118, 153 (1983),