所有图片(2)
别名:
(2R,3R)-1,2,3,4-丁四醇
线性分子式:
HOCH2[CH(OH)]2CH2OH
CAS号:
分子量:
122.12
Beilstein:
1719752
MDL编号:
UNSPSC代码:
12352201
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
检测方案
99%
形式
solid
旋光性
[α]20/D −14°, c = 2 in ethanol
mp
88-90 °C (lit.)
SMILES字符串
OC[C@@H](O)[C@H](O)CO
InChI
1S/C4H10O4/c5-1-3(7)4(8)2-6/h3-8H,1-2H2/t3-,4-/m1/s1
InChI key
UNXHWFMMPAWVPI-QWWZWVQMSA-N
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警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
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Physical review letters, 88(9), 095701-095701 (2002-02-28)
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F Bravo et al.
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Differently protected erythro and threo furanoid glycals were synthesized by selenoxide elimination when phenyl 1-selenoglycosides were treated in oxidizing conditions (tBuOOH, Ti(O(i)Pr)(4), Et(2)(i)PrN). The phenyl 1-selenoglycosides were obtained from methyl 2-deoxy-D-erythro-pentofuranoside by protection of the primary hydroxyl or both hydroxyls
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