您当前所在的位置:首页 > 产品中心 > 产品信息
Acetobromo-α-D-glucose_分子结构_CAS_572-09-8)
点击图片或这里关闭

Acetobromo-α-D-glucose

产品号 00530 公司名称 Sigma Aldrich
CAS号 572-09-8 公司网站 http://www.sigmaaldrich.com
分子式 C14H19BrO9 电 话 1-800-521-8956
分子量 411.19926 传 真
纯 度 ≥95.0% (AT) 电子邮件
保 存 Chembase数据库ID: 104038

产品价格信息

请登录

产品别名

标题
Acetobromo-α-D-glucose
IUPAC标准名
[(2R,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-bromooxan-2-yl]methyl acetate
IUPAC传统名
[(2R,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-bromooxan-2-yl]methyl acetate
别名
1-Bromo-α-D-glucose tetraacetate
2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl bromide

产品登记号

MDL号 MFCD00063254
PubChem SID 24845061
Beilstein号 96669
CAS号 572-09-8

产品性质

其他组分 ~1% CaCO3 as stabilizer
Empirical Formula (Hill Notation) C14H19BrO9
级别 purum
纯度 ≥95.0% (AT)
运输包装 dry ice
熔点 86-89 °C
比旋光度 [α]20/D +195±10°, c = 3% in chloroform
MSDS下载 下载链接
个人保护装置 Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
保存温度 -20°C
德国WGK号 nwg

产品详细信息

详细说明 (English)
Other Notes
Glucose derivative used for the β-glucosylation of alcohols (Königs-Knorr synthesis) in the presence of an activator, e.g. metal salts 1,2,3; Radical substitution at C-14
Application
Acetobromo-α-D-glucose is used as a possible poly (ethylene terephthalate) (PET) surface modification reagent to increase its blood compatibility.
详细说明 (简体中文)
Other Notes
Glucose derivative used for the β-glucosylation of alcohols (Königs-Knorr synthesis) in the presence of an activator, e.g. metal salts 1,2,3; Radical substitution at C-14
Application
Acetobromo-α-D-glucose is used as a possible poly (ethylene terephthalate) (PET) surface modification reagent to increase its blood compatibility.

参考文献