摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

[14C]-Sodium cyanide | 3396-82-5

中文名称
——
中文别名
——
英文名称
[14C]-Sodium cyanide
英文别名
sodium 14C-cyanide;<14C>-Sodium cyanide;<14C>sodium cyanide;Sodium <14C>cyanide;sodium<14C>cyanide;sodium carbon-14 cyanide;[(14)C]sodium cyanide
[14C]-Sodium cyanide化学式
CAS
3396-82-5
化学式
CNNa
mdl
——
分子量
50.9965
InChiKey
RTVFYQXEHKQMKO-DEQYMQKBSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -0.36
  • 重原子数:
    3.0
  • 可旋转键数:
    0.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    23.79
  • 氢给体数:
    0.0
  • 氢受体数:
    1.0

SDS

SDS:fc2447dc3485378d20cf65b53be9e173
查看

反应信息

  • 作为反应物:
    参考文献:
    名称:
    866.苯酚的氧化和生物合成。第六部分 芳科生物碱的生物发生
    摘要:
    DOI:
    10.1039/jr9630004545
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 sodium azide 作用下, 生成 [14C]-Sodium cyanide
    参考文献:
    名称:
    A RAPID METHOD OF PREPARING NaC14N FROM BaC14O3
    摘要:
    DOI:
    10.1021/ja01202a514
点击查看最新优质反应信息

文献信息

  • A small-scale synthesis and enantiomeric resolution of (RS)-[1-14C]-2-Phenylpropionic acid and biosynthesis of its diastereomeric acyl glucuronides
    作者:David M. Shackleford、Peter J. Hayball、Geoffrey D. Reynolds、David P.G. Hamon、Allan M. Evans、Robert W. Milne、Roger L. Nation
    DOI:10.1002/jlcr.450
    日期:2001.3.15
    David M. Shackleford, Peter J. Hayball, Geoffrey D. Reynolds, David P.G. Hamon, Allan M. Evans, Robert W. Milne, Roger L. Nation
    David M. Shackleford、Peter J. Hayball、Geoffrey D. Reynolds、David PG Hamon、Allan M. Evans、Robert W. Milne、Roger L. Nation
  • A Simplified Synthesis of the Diastereomers of Levuglandin E<sub>2</sub>
    作者:Venkataraman Amarnath、Kalyani Amarnath、Tina Masterson、Sean Davies、L. Jackson Roberts
    DOI:10.1081/scc-200048945
    日期:2005.1.1
    report a synthesis of Levuglandin E2, as a mixture of easily separable diastereomers (15‐E2‐isoketals). The key feature is the protection of its reactive aldehyde as dimethyl acetal, which is introduced with 2,2‐dimethoxyethanal and removed in minutes with Montmorillonite K‐10. The synthesis could be modified to the preparation of 15‐E2‐isoketals with stable isotopes or with radiolabels.
    摘要 我们报告了 Levuglandin E2 的合成,作为易于分离的非对映异构体 (15-E2-isoketals) 的混合物。关键特征是将其反应性醛保护为二甲基乙缩醛,通过 2,2-二甲氧基乙醛引入,并在几分钟内用蒙脱石 K-10 去除。合成可以修改为具有稳定同位素或放射性标记的 15-E2-isoketals 的制备。
  • Synthesis of14C-labeled 4-hydroxyindole as an intermediate for the preparation of (S)-2-[4-[2-[3-(indol-2-[14C]-4-yloxy)-2-hydroxypropylamino]-2-methylpropyl]-phenoxy]pyridine-5-carboxamide (LY368842-[indole-14C]) glycolate
    作者:Boris A. Czeskis、Dean K. Clodfelter、William J. Wheeler
    DOI:10.1002/jlcr.631
    日期:2002.11
    Synthesis of 4-hydroxyindole labeled with 14C at the 2-position was accomplished based on the vicarious nucleophilic substitution reaction of benzyl-protected 3-nitrophenol with p-chlorophenoxyacetonitrile-[1-14C]. This was followed by the reductive cyclization of o-nitrocyanomethyl derivative by palladium catalyzed hydrogenation. p-Chlorophenoxyacetonitrile-[1-14C] was prepared from commercially available p-chlorophenoxymethyl chloride and sodium cyanide-[14C]. 4-Hydroxyindole-[2-14C] was used for the synthesis of 14C-labeled β3 adrenergic agonist LY368842. Copyright © 2002 John Wiley & Sons, Ltd.
    合成2位标记有14C的4-羟基吲哚是通过苄基保护的3-硝基苯与对氯苯氧基乙腈-[1-14C]进行替代亲核反应实现的。之后,通过催化氢化反应对邻硝基氰基甲基衍生物进行还原环化。对氯苯氧基乙腈-[1-14C]是由市售的对氯苯氧基甲基氯氰化钠-[14C]合成的。4-羟基吲哚-[2-14C]被用于合成14C标记的β3肾上腺素能激动剂LY368842。版权 © 2002 约翰·威利父子公司。
  • The acid-catalyzed dehydration of (methyl β-d-glycero-d-gulo-heptopyranosid)uronic acid
    作者:Christian D. Cottet、Milton S. Feather
    DOI:10.1016/s0008-6215(00)80812-5
    日期:1981.12
    organic solvents, isolated by hydrolysis and subsequent dehydration of (methyl β- d - glycero - d - gulo -heptopyranosid)uronic acid ( 1 ) in m sulfuric acid solution at 100°, is 5-hydroxymethyl-2-furaldehyde ( 2 ), presumably produced via loss of C-7 by decarboxylation. The mechanism of the conversion was studied by synthesis of the [1- 14 C] 1 and conversion to 5-hydroxymethyl-2-fur[ 14 C]aldehyde (
    摘要可溶于有机溶剂的主要产物是5-羟甲基-2 -呋喃甲醛(2),大概是通过脱羧使C-7损失而产生的。通过合成[1-1-14 C] 1并转化为5-羟甲基-2-呋喃[14 C]醛(2-14 C),研究了转化机理。在酸化的D 2 O中将1转化为2-14 C,然后通过1 Hn.mr-ms测量C结合的D,表明2-14 C仅在呋喃的D-3(40原子%)处标记戒指。溶性物质的主要部分(以毫秒为单位)显示为d-甘油-d-gulo-庚糖醛酸和由1的解产生的内酯。
  • Preparation of carbon-14 labelled guazatine
    作者:Harry R. Hudson、Fatima Ismail、Lubomira Powroznyk
    DOI:10.1002/jlcr.487
    日期:2001.6
    for the manufacture of guazatine, an agrochemical fungicide comprising a mixture of guanidated di-, tri-, and poly-amines derived from octamethylenediamine. The product has been prepared with carbon-14 labelling of the terminal positions of the octamethylene chains. Copyright © 2001 John Wiley & Sons, Ltd.
    描述了一种用于制造丁胺的工业过程的小规模实验室模拟方法,丁胺是一种农用化学杀真菌剂,包含衍生自八亚甲基二胺的化二胺、三胺和多胺的混合物。该产品是用八亚甲基链末端位置的碳 14 标记制备的。版权所有 © 2001 John Wiley & Sons, Ltd.
查看更多