卡西酮盐酸盐
卡西酮盐酸盐结构式
|
常用名 | 卡西酮盐酸盐 | 英文名 | r(+)-cathinone hydrochloride |
|---|---|---|---|---|
| CAS号 | 76333-53-4 | 分子量 | 185.65100 | |
| 密度 | N/A | 沸点 | 255ºC at 760 mmHg | |
| 分子式 | C9H12ClNO | 熔点 | 189-190ºC | |
| MSDS | N/A | 闪点 | 108ºC | |
| 符号 |
GHS02, GHS06, GHS08 |
信号词 | Danger |
| 中文名 | 卡西酮盐酸盐 |
|---|---|
| 英文名 | (2R)-2-amino-1-phenylpropan-1-one,hydrochloride |
| 中文别名 | 卡西酮 盐酸盐 |
| 沸点 | 255ºC at 760 mmHg |
|---|---|
| 熔点 | 189-190ºC |
| 分子式 | C9H12ClNO |
| 分子量 | 185.65100 |
| 闪点 | 108ºC |
| 精确质量 | 185.06100 |
| PSA | 43.09000 |
| LogP | 2.71880 |
| 储存条件 | ?20°C |
| 符号 |
GHS02, GHS06, GHS08 |
|---|---|
| 信号词 | Danger |
| 危害声明 | H225-H301 + H311 + H331-H370 |
| 警示性声明 | P210-P260-P280-P301 + P310-P311 |
| 危害码 (欧洲) | F,T |
| 风险声明 (欧洲) | 11-23/24/25-39/23/24/25 |
| 安全声明 (欧洲) | 7-16-36/37-45 |
| 危险品运输编码 | UN1230 - class 3 - PG 2 - Methanol, solution |
|
~96%
卡西酮盐酸盐 76333-53-4 |
| 文献：Besse; Veschambre; Dickman; Chenevert Journal of Organic Chemistry, 1994 , vol. 59, # 26 p. 8288 - 8291 |
|
~69%
卡西酮盐酸盐 76333-53-4 |
| 文献：Berrang; Lewin; Carroll Journal of Organic Chemistry, 1982 , vol. 47, # 13 p. 2643 - 2647 |
|
~%
卡西酮盐酸盐 76333-53-4 |
| 文献：Hwang, Gweon Il; Chung, Jae-Ho; Lee, Won Koo Tetrahedron, 1996 , vol. 52, # 37 p. 12111 - 12116 |
|
~%
卡西酮盐酸盐 76333-53-4 |
| 文献：Besse; Veschambre; Dickman; Chenevert Journal of Organic Chemistry, 1994 , vol. 59, # 26 p. 8288 - 8291 |
|
~%
卡西酮盐酸盐 76333-53-4 |
| 文献：Besse; Veschambre; Dickman; Chenevert Journal of Organic Chemistry, 1994 , vol. 59, # 26 p. 8288 - 8291 |
|
~%
卡西酮盐酸盐 76333-53-4 |
| 文献：Berrang; Lewin; Carroll Journal of Organic Chemistry, 1982 , vol. 47, # 13 p. 2643 - 2647 |
|
~%
卡西酮盐酸盐 76333-53-4 |
| 文献：Berrang; Lewin; Carroll Journal of Organic Chemistry, 1982 , vol. 47, # 13 p. 2643 - 2647 |
|
~%
卡西酮盐酸盐 76333-53-4 |
| 文献：Besse; Veschambre; Dickman; Chenevert Journal of Organic Chemistry, 1994 , vol. 59, # 26 p. 8288 - 8291 |
|
~%
卡西酮盐酸盐 76333-53-4 |
| 文献：Besse; Veschambre; Dickman; Chenevert Journal of Organic Chemistry, 1994 , vol. 59, # 26 p. 8288 - 8291 |
|
Utilization of micellar electrokinetic chromatography-tandem mass spectrometry employed volatile micellar phase in the analysis of cathinone designer drugs.
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A new drug war.
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Recreational drug discovery: natural products as lead structures for the synthesis of smart drugs.
Nat. Prod. Rep. 31(7) , 880-904, (2014) Covering: up to December 2013. Over the past decade, there has been a growing transition in recreational drugs from natural materials (marijuana, hashish, opium), natural products (morphine, cocaine),... |
