tert-Butyl (3-aminopropyl)carbamate structure
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Common Name | tert-Butyl (3-aminopropyl)carbamate | ||
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CAS Number | 75178-96-0 | Molecular Weight | 174.24 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 271.7±23.0 °C at 760 mmHg | |
Molecular Formula | C8H18N2O2 | Melting Point | 22 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 118.1±22.6 °C | |
Symbol |
GHS05, GHS07 |
Signal Word | Danger |
Use of tert-Butyl (3-aminopropyl)carbamatetert-Butyl (3-aminopropyl)carbamate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | N-Boc-1,3-propanediamine |
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Synonym | More Synonyms |
Description | tert-Butyl (3-aminopropyl)carbamate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog | |
In Vitro | N-Boc-1,3-propanediamine 在亚精胺类似物的合成和铃木反应中起着关键作用。 |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 271.7±23.0 °C at 760 mmHg |
Melting Point | 22 °C(lit.) |
Molecular Formula | C8H18N2O2 |
Molecular Weight | 174.24 |
Flash Point | 118.1±22.6 °C |
Exact Mass | 174.136826 |
PSA | 64.35000 |
LogP | 0.76 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.456 |
Symbol |
GHS05, GHS07 |
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Signal Word | Danger |
Hazard Statements | H302-H314 |
Precautionary Statements | P280-P305 + P351 + P338-P310 |
Personal Protective Equipment | Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | C:Corrosive |
Risk Phrases | R22;R34 |
Safety Phrases | S26-S36/37/39-S45 |
RIDADR | UN 3259 8/PG 3 |
WGK Germany | 3 |
Packaging Group | III |
Hazard Class | 8 |
HS Code | 2924199090 |
Precursor 8 | |
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DownStream 6 | |
HS Code | 2924199090 |
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Summary | 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
Inhibition of N8-acetylspermidine deacetylase by active-site-directed metal coordinating inhibitors.
J. Med. Chem. 35 , 2414, (1992) A number of substrate analogues of N8-acetylspermidine (N8-AcSpd) (16) and chemical modifying agents containing metal coordinating ligands were assayed as inhibitors of the cytoplasmic enzyme N8-AcSpd... |
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B. Plouvier et al.
Heterocycles 32 , 693, (1991)
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Carbamic acid, N-(3-aminopropyl)-, 1,1-dimethylethyl ester |
2-Methyl-2-propanyl (3-aminopropyl)carbamate |
MFCD00210021 |
tert-butyl N-(3-aminopropyl)carbamate |
N-(3-Aminopropyl)carbamicacidtertbutylester |