Name | (RS)-3-(2-Carboxypiperazin-4-yl)-propyl-1-phosphonicacid |
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Synonyms |
3-2-Cpp
DL-CPP |
Description | (RS)-CPP ((±)-CPP) is a potent and selective NMDA antagonist. (RS)-CPP inhibits central neuron responses, and has anticonvulsant activity[1]. |
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Related Catalog | |
References |
Density | 1.408g/cm3 |
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Boiling Point | 546.7ºC at 760mmHg |
Molecular Formula | C8H17N2O5P |
Molecular Weight | 252.20 |
Flash Point | 284.4ºC |
Exact Mass | 252.08800 |
PSA | 119.91000 |
Vapour Pressure | 2.14E-13mmHg at 25°C |
Index of Refraction | 1.53 |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi: Irritant; |
Risk Phrases | 36/37/38 |
Safety Phrases | 22-26-36 |
RIDADR | NONH for all modes of transport |
~76% 100828-16-8 |
Literature: Demaine; Smith Synthesis, 1992 , # 11 p. 1065 - 1067 |
~% 100828-16-8 |
Literature: British Technology Group Limited Patent: US5399693 A1, 1995 ; |
~% 100828-16-8 |
Literature: Demaine; Smith Synthesis, 1992 , # 11 p. 1065 - 1067 |
~75% 100828-16-8 |
Literature: Demaine; Smith Synthesis, 1992 , # 11 p. 1065 - 1067 |
~% 100828-16-8 |
Literature: Pevarello, P.; Scappi, G.; Varasi, M. Organic Preparations and Procedures International, 1994 , vol. 26, # 3 p. 366 - 370 |
~% 100828-16-8 |
Literature: Demaine; Smith Synthesis, 1992 , # 11 p. 1065 - 1067 |
~% 100828-16-8 |
Literature: Pevarello, P.; Scappi, G.; Varasi, M. Organic Preparations and Procedures International, 1994 , vol. 26, # 3 p. 366 - 370 |
Precursor 7 | |
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DownStream 0 |