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

2-异丙基苯基异硫氰酸酯 | 36176-31-5

中文名称
2-异丙基苯基异硫氰酸酯
中文别名
2-异丙基苯基硫代异氰酸酯
英文名称
2-isopropylphenyl isothiocyanate
英文别名
1-isopropyl-2-isothiocyanatobenzene;1-isothiocyanato-2-propan-2-ylbenzene
2-异丙基苯基异硫氰酸酯化学式
CAS
36176-31-5
化学式
C10H11NS
mdl
MFCD00022053
分子量
177.27
InChiKey
QQOOMDSEMQHMIR-UHFFFAOYSA-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

物化性质

  • 沸点:
    131 °C
  • 密度:
    1.05
  • 闪点:
    131-132°C/10mm
  • 稳定性/保质期:
    常规情况下不会分解,没有危险反应。

计算性质

  • 辛醇/水分配系数(LogP):
    4.4
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    44.4
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 危险等级:
    8
  • 危险品标志:
    Xn
  • 危险类别码:
    R20/21/22,R36/37/38
  • 危险品运输编号:
    2810
  • 海关编码:
    2930909090
  • 包装等级:
    III
  • 危险类别:
    8
  • 安全说明:
    S23,S36/37/39,S45
  • 储存条件:
    密封、阴凉、干燥、通风保存。

SDS

SDS:18bf086b267dcd6cba27b24b5025564c
查看
Name: 2-Isopropylphenyl isothiocyanate 95+% Material Safety Data Sheet
Synonym:
CAS: 36176-31-5
Section 1 - Chemical Product MSDS Name:2-Isopropylphenyl isothiocyanate 95+% Material Safety Data Sheet
Synonym:

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
36176-31-5 2-Isopropylphenyl isothiocyanate 95+% unlisted
Hazard Symbols: XN
Risk Phrases: 20/21/22 36/37/38

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Harmful by inhalation, in contact with skin and if swallowed.
Irritating to eyes, respiratory system and skin.Moisture sensitive.
Potential Health Effects
Eye:
Causes eye irritation. Lachrymator (substance which increases the flow of tears).
Skin:
Causes skin irritation. Harmful if absorbed through the skin.
Ingestion:
Harmful if swallowed. May cause irritation of the digestive tract.
Inhalation:
Harmful if inhaled. Causes respiratory tract irritation.
Chronic:
Not available.

Section 4 - FIRST AID MEASURES
Eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid.
Skin:
Get medical aid. Flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes.
Ingestion:
Get medical aid. Wash mouth out with water.
Inhalation:
Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical aid.
Notes to Physician:
Treat symptomatically and supportively.

Section 5 - FIRE FIGHTING MEASURES
General Information:
As in any fire, wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear.
Extinguishing Media:
Use foam, dry chemical, or carbon dioxide.

Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Absorb spill with inert material (e.g. vermiculite, sand or earth), then place in suitable container.

Section 7 - HANDLING and STORAGE
Handling:
Avoid breathing dust, vapor, mist, or gas. Avoid contact with skin and eyes. Use only in a chemical fume hood.
Storage:
Keep refrigerated. (Store below 4C/39F.) Store in a tightly closed container. Store in a dry area. Store under nitrogen.

Section 8 - EXPOSURE CONTROLS, PERSONAL PROTECTION
Engineering Controls:
Facilities storing or utilizing this material should be equipped with an eyewash facility and a safety shower. Use adequate ventilation to keep airborne concentrations low.
Exposure Limits CAS# 36176-31-5: Personal Protective Equipment Eyes: Not available.
Skin:
Wear appropriate protective gloves to prevent skin exposure.
Clothing:
Wear appropriate protective clothing to prevent skin exposure.
Respirators:
Follow the OSHA respirator regulations found in 29 CFR 1910.134 or European Standard EN 149. Use a NIOSH/MSHA or European Standard EN 149 approved respirator if exposure limits are exceeded or if irritation or other symptoms are experienced.

Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Liquid
Color: colorless
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: 131 - 132 deg C @10mmHg
Freezing/Melting Point: Not available.
Autoignition Temperature: Not available.
Flash Point: Not available.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature:
Solubility in water:
Specific Gravity/Density: 1.05
Molecular Formula: C10H11NS
Molecular Weight: 177

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Not available.
Conditions to Avoid:
Incompatible materials, exposure to moist air or water.
Incompatibilities with Other Materials:
Strong oxidizing agents, acids, bases.
Hazardous Decomposition Products:
Nitrogen oxides, carbon monoxide, oxides of sulfur, carbon dioxide, acrid smoke and fumes.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 36176-31-5 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
2-Isopropylphenyl isothiocyanate - Not listed by ACGIH, IARC, or NTP.

Section 12 - ECOLOGICAL INFORMATION


Section 13 - DISPOSAL CONSIDERATIONS
Dispose of in a manner consistent with federal, state, and local regulations.

Section 14 - TRANSPORT INFORMATION

IATA
Shipping Name: TOXIC LIQUID, ORGANIC, N.O.S.*
Hazard Class: 6.1
UN Number: 2810
Packing Group: III
IMO
Shipping Name: TOXIC LIQUID, ORGANIC, N.O.S.
Hazard Class: 6.1
UN Number: 2810
Packing Group: III
RID/ADR
Shipping Name: TOXIC LIQUID, ORGANIC, N.O.S.
Hazard Class: 6.1
UN Number: 2810
Packing group: III

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: XN
Risk Phrases:
R 20/21/22 Harmful by inhalation, in contact with
skin and if swallowed.
R 36/37/38 Irritating to eyes, respiratory system
and skin.
Safety Phrases:
S 26 In case of contact with eyes, rinse immediately
with plenty of water and seek medical advice.
S 36/37/39 Wear suitable protective clothing, gloves
and eye/face protection.
WGK (Water Danger/Protection)
CAS# 36176-31-5: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 36176-31-5 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 36176-31-5 is not listed on the TSCA inventory.
It is for research and development use only.


SECTION 16 - ADDITIONAL INFORMATION
N/A

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    2-Arylimino-5,6-dihydro-4H-1,3-thiazines as a new class of cannabinoid receptor agonists. Part 1: Discovery of CB2 receptor selective compounds
    摘要:
    2-Arylimino-5,6-dihydro-4H-1,3-thiazines have been identified as a novel class of cannabinoid agonists. A lead structure with moderate activity was discovered through a high throughput screening assay. Structure-activity relationships led to the discovery of potent agonists of CB2 receptor. The most potent compound 13 displays K-i values of > 5000 and 9 nM to CB1 and CB2 receptors, respectively. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.04.093
  • 作为产物:
    描述:
    二硫化碳2-异丙基苯胺三乙胺氯甲酸乙酯 作用下, 以 甲苯二氯甲烷 为溶剂, 反应 14.17h, 以99%的产率得到2-异丙基苯基异硫氰酸酯
    参考文献:
    名称:
    MEDICINAL COMPOSITION CONTAINING 1,3-THIAZINE DERIVATIVE
    摘要:
    公开号:
    EP1375489B1
点击查看最新优质反应信息

文献信息

  • [EN] PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO<br/>[FR] COMPOSITIONS PESTICIDES ET PROCÉDÉS RELATIFS À CES COMPOSITIONS
    申请人:DOW AGROSCIENCES LLC
    公开号:WO2013009791A1
    公开(公告)日:2013-01-17
    This document discloses molecules having the following formula ("Formula One") The molecules disclosed in this document are related to the field of processes to produce molecules that are useful as pesticides (e.g., acaricides, insecticides, molluscicides, and nematicides), such molecules, and processes of using such molecules to control pests.
    这份文件公开了具有以下公式(“公式一”)的分子。本文档中披露的分子与生产作为农药(例如,杀螨剂、杀虫剂、杀软体动物剂和杀线虫剂)有用的分子的过程领域有关,以及这样的分子和使用这样的分子控制害虫的过程。
  • Structure-Based Design, Parallel Synthesis, Structure−Activity Relationship, and Molecular Modeling Studies of Thiocarbamates, New Potent Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitor Isosteres of Phenethylthiazolylthiourea Derivatives
    作者:Angelo Ranise、Andrea Spallarossa、Sara Cesarini、Francesco Bondavalli、Silvia Schenone、Olga Bruno、Giulia Menozzi、Paola Fossa、Luisa Mosti、Massimiliano La Colla、Giuseppina Sanna、Marta Murreddu、Gabriella Collu、Bernardetta Busonera、Maria Elena Marongiu、Alessandra Pani、Paolo La Colla、Roberta Loddo
    DOI:10.1021/jm049252r
    日期:2005.6.1
    In this paper we describe our structure-based ligand design, synthetic strategy, and structure-activity relationship (SAR) studies that led to the identification of thiocarbamates (TCs), a novel class of non-nucleoside reverse transcriptase inhibitors (NNRTIs), isosteres of phenethylthiazolylthiourea (PETT) derivatives. Assuming as a lead compound O-[2-(phthalimido)ethyl]phenylthiocarbamate 12, one
    在本文中,我们描述了我们基于结构的配体设计,合成策略和结构与活性关系(SAR)的研究,这些研究导致了硫代氨基甲酸酯(TC)的鉴定,这是一类新型的非核苷类逆转录酶抑制剂(NNRTIs),等位基因苯乙基噻唑基硫脲(PETT)衍生物的制备。假设O- [2-(邻苯二甲酰亚胺基)乙基]苯基硫代氨基甲酸酯为先导化合物,前述酰基硫代氨基甲酸酯的前体之一(Ranise,A .;等人,J。Med。Chem。2003,46,768-781) ,通过平行合成制备了两个目标溶液相TC库。领先的优化策略导致对位取代的TC 31、33、34、39、40、41、44、45和50在纳摩尔浓度的基于MT-4的测定中对野生型HIV-1具有活性( EC50范围:0.04-0.01 microM)。最有效的同类物50(EC50 = 0。01 microM)在邻苯二甲酰亚胺部分的第4位带有一个甲基,在N-苯环的对位带有一个硝基。大
  • Di-tert-butyl peroxide (DTBP)-mediated synthesis of symmetrical <i>N</i>,<i>N</i>′-disubstituted urea/thiourea motifs from isothiocyanates in water
    作者:Jinchen Yang、Ling Chen、Yibo Dong、Jinli Zhang、Yangjie Wu
    DOI:10.1080/00397911.2021.2001017
    日期:2022.1.2
    ABATRACT A direct approach to N,N-disubstituted urea/thiourea from the self-condensation reactions of isothiocyanates in water has been developed. This access tolerated a wide range of functional groups on the aromatic ring, providing a practical and environment-friendly process to N,N-disubstituted urea/thiourea in moderate to excellent yields from safe and easily available starting materials. A
    ABATRACT 已经开发了一种从异硫氰酸酯在水中的自缩合反应直接得到N , N '-二取代脲/硫脲的方法。这种访问容忍了芳环上的多种官能团,为N , N '-二取代脲/硫脲提供了一种实用且环境友好的工艺,从安全且易于获得的起始材料以中等至优异的产率。还提出了尿素脱硫自缩合反应的合理机理,并借助中间体研究的 ESI 质谱分析证明了二叔丁基过氧化物 (DTBP) 和铜催化剂在本策略中的作用。
  • [EN] PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO<br/>[FR] COMPOSITIONS PESTICIDES ET PROCÉDÉS CORRESPONDANTS
    申请人:DOW AGROSCIENCES LLC
    公开号:WO2014011429A1
    公开(公告)日:2014-01-16
    This document discloses molecules having the following formula ("Formula One"). The molecules disclosed in this document are related to the field of processes to produce molecules that are useful as pesticides (e.g., acaricides, insecticides, molluscicides, and nematicides), such molecules, and processes of using such molecules to control pests.
    这份文件公开了具有以下公式(“公式一”)的分子。本文档中披露的分子与生产作为农药(例如,杀螨剂、杀虫剂、杀软体动物剂和杀线虫剂)有用的分子的过程领域有关,以及这些分子,以及使用这些分子控制害虫的过程。
  • MOLECULES HAVING CERTAIN PESTICIDAL UTILITIES, INTERMEDIATES, COMPOSITIONS, AND PROCESSES, RELATED THERETO
    申请人:Dow AgroSciences LLC
    公开号:US20160021883A1
    公开(公告)日:2016-01-28
    This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such molecules and intermediates used in such processes, compositions containing such molecules, and processes of using such molecules against such pests. These molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses molecules having the following formula (“Formula One”).
    这份披露涉及具有对线虫门、节肢动物门和/或软体动物门害虫有用的分子领域,用于生产这种分子和用于这种过程的中间体的过程,含有这种分子的组合物,以及使用这种分子对抗这些害虫的过程。这些分子可以用作线虫杀虫剂、螨虫杀虫剂、杀虫剂、螨虫剂和/或软体动物杀虫剂。本文件披露了具有以下式(“式一”)的分子。
查看更多

表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
查看更多图谱数据,请前往“摩熵化学”平台
mass
查看更多图谱数据,请前往“摩熵化学”平台
ir
查看更多图谱数据,请前往“摩熵化学”平台
  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
查看更多图谱数据,请前往“摩熵化学”平台
Assign
Shift(ppm)
查看更多图谱数据,请前往“摩熵化学”平台
测试频率
样品用量
溶剂
溶剂用量
查看更多图谱数据,请前往“摩熵化学”平台

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐