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雷洛昔芬

CAS 84449-90-1C28H27NO4SMW 473.6

雷洛昔芬(CAS 84449-90-1):分子式 C28H27NO4S、分子量 473.6;类别 有机化学品。

产品描述

雷洛昔芬(CAS 84449-90-1)是一种有机化学品原料。其分子式 C28H27NO4S 由 28 个碳、27 个氢、1 个氮、4 个氧、1 个硫 组成。 分子量约为 473.6。公开物性数据显示其熔点约 268-272、LogP 约 5.2。作为化工品采购代理与分销渠道,我们可在国内及跨境渠道为雷洛昔芬寻源比价,并安排小批量试样与批次采购;下单前提供完整 COA、质检报告与合规文件,验收以批次 COA 为准。

规格参数

CAS号84449-90-1
分子式C28H27NO4S
分子量473.6
熔点268-272
LogP5.2
应用领域Estrogen Antagonists、Selective Estrogen Receptor Modulators、Bone Density Conservation Agents、MEDICATION、Pharmaceuticals、Methods of Manufacturing: Condensation of alpha-bromo-p-methoxyacetophenone with m-methoxythiophenol using polyphosphoric acid yields alpha-(m-methoxyphenylthio)-p-methoxy-acetophenone
类别有机化学品

用途与场景

登记用途:Estrogen Antagonists、Selective Estrogen Receptor Modulators、Bone Density Conservation Agents、MEDICATION、Pharmaceuticals、Methods of Manufacturing: Condensation of alpha-bromo-p-methoxyacetophenone with m-methoxythiophenol using polyphosphoric acid yields alpha-(m-methoxyphenylthio)-p-methoxy-acetophenone。

采购档案

这个产品是什么

雷洛昔芬 是一种以碳骨架为基础的有机化合物,登记 CAS 号为 84449-90-1,分子式 C28H27NO4S(分子量 473.6),归属于有机化学品大类化工原料。

识别信息

登记 CAS 号:84449-90-1

其分子式 C28H27NO4S 由 28 个碳、27 个氢、1 个氮、4 个氧、1 个硫 组成。

别名/同义词:雷洛昔芬 · Raloxifene

所属分类:有机化学品

常见问题

雷洛昔芬 的 CAS 号是多少?

雷洛昔芬 的 CAS 登记号为 84449-90-1。

雷洛昔芬 的分子式与分子量是多少?

分子式 C28H27NO4S,分子量 473.6。

雷洛昔芬 还有哪些别名?

别名/同义词:雷洛昔芬、Raloxifene。

雷洛昔芬 的登记用途是什么?

登记用途:Estrogen Antagonists、Selective Estrogen Receptor Modulators、Bone Density Conservation Agents、MEDICATION、Pharmaceuticals、Methods of Manufacturing: Condensation of alpha-bromo-p-methoxyacetophenone with m-methoxythiophenol using polyphosphoric acid yields alpha-(m-methoxyphenylthio)-p-methoxy-acetophenone。

雷洛昔芬 属于哪个分类?

所属分类:有机化学品。

如何在 591daili.cn 采购 雷洛昔芬?

请在联系页面提交产品名称、CAS 号与数量,我们作为采购代理在国内及跨境渠道为您寻源比价,安排试样与批次采购,下单前提供 COA 与合规文件。

包装与单证

包装按订单确认,从实验室小包装到吨袋大货,随订单安排而非在页面上写死。每批随货附 COA 分析证书,可另提供 MSDS;若终端用途带有法规限度(食品接触、药品或化妆品),请在询价时说明执行标准,等级按该标准确定。

PubChem 公开数据

雷洛昔芬(CAS 84449-90-1)的公开数据库记录,列此仅供独立核对。

危险化学品分类与危害说明

Reported hazard statementsH302 (33.3%), H311 (66.7%), H315 (33.3%), H319 (33.3%), H332 (33.3%), H335 (33.3%), H360 (66.7%), H411 (66.7%)

H302 (33.3%): Harmful if swallowed [Warning Acute toxicity, oral]

H311 (66.7%): Toxic in contact with skin [Danger Acute toxicity, dermal]

物理形态与操作说明

  • Solid
  • Crystals from acetone
  • Crystals from methanol/water; mp: 258 °C; UV max (ethanol): 286 nm (epsilon 32800). Freely soluble in dimethylsulfoxide; sparingly soluble in methanol; slightly soluble in alcohol; very slightly soluble in water, isopropyl alcohol, octanol. Practically insoluble in ether, ethyl acetate /Raloxifene hydrochloride/
  • Insoluble
  • Stable under recommended storage conditions. /Raloxifene hydrochloride/
  • 213.4 Ų [M-H]- [CCS Type: DT; Buffer gas: N2; Ionization: ESI-; Dataset: TOXCAST; Source Identifier: DTXSID1034181]

公开数据库收录的理化数据

熔点268-272
熔点143-147 °C
熔点143 - 147 °C
溶解度5.12e-04 g/L
LogP5.2
LogP4.48

这个物质在各数据库里的编号

CAS Registry Number84449-90-1
PubChem CID5035
分子式C28H27NO4S
IUPAC 名称[6-hydroxy-2-(4-hydroxyphenyl)-1-benzothiophen-3-yl]-[4-(2-piperidin-1-ylethoxy)phenyl]methanone
UNII(FDA)YX9162EO3I

数据库记载的用途

  • Estrogen Antagonists; Selective Estrogen Receptor Modulators; Bone 密度 Conservation Agents
  • Preparation ... C. D. Jones, European Patent Office patent 62503; idem, United States of America patent 4418068 (1982, 1983 both to Lilly).
  • Indicated for the prevention and treatment of osteoporosis in postmenopausal women, as well as prevention and treatment of corticosteroid-induced bone loss. Indicated for the reduction in the risk of invasive breast cancer in postmenopausal women with osteoporosis or postmenopausal women with a high risk for invasive breast cancer.
  • Raloxifene is an FDA-approved second-generation selective estrogen receptor modulator (SERM) that exerts estrogen-agonistic effects on bone, increasing bone mineral density and mass by decreasing bone resorption, and it is indicated for the treatment and prevention of postmenopausal osteoporosis. Raloxifene is also indicated for the reduction of risk of invasive breast cancer in postmenopausal women who are at high risk for invasive breast cancer or who have osteoporosis, with high risk defined as having 1 or more
  • Evista is indicated for the treatment and prevention of osteoporosis in postmenopausal women. /Included in US product label/
  • Evista is indicated for the reduction in risk of invasive breast cancer in postmenopausal women with osteoporosis. /Included in US product label/

它在各数据库里的别名

raloxifene; 84449-90-1; Keoxifene; Raloxifeno; Raloxifenum; Raloxifenum [Latin]; Raloxiphene; LY-139481; Eviden; Raxeto; LY 139481; DTXSID3023550; NSC-747974; YX9162EO3I; J22.982B; (2-(4-Hydroxyphenyl)-6-hydroxybenzo(b)thien-3-yl)(4-(2-(1-piperidinyl)ethoxy)phenyl)methanone

计算机算出的分子描述符

分子量473.6
XLogP36.1
氢键供体数2
氢键受体数6
可旋转键数7
精确质量473.16607952
单同位素质量473.16607952
拓扑极性表面积98.2
重原子数34
形式电荷0

数据库摘要

Raloxifene · CAS 84449-90-1 · C28H27NO4S. UNII YX9162EO3I. 熔点: 268-272; 熔点: 143-147 °C; 熔点: 143 - 147 °C.

数据来源:PubChem / Wikidata;与随货 COA 不一致时以 COA 为准。

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