1-Boc-2-isopropylhydrazine
- Product Name
- 1-Boc-2-isopropylhydrazine
- CAS No.
- 16689-35-3
- Chemical Name
- 1-Boc-2-isopropylhydrazine
- Synonyms
- 1-Boc-2-isopropylhydrazine;tert-Butyl 3-(Isopropyl)carbazate;tert-Butyl 3-(Isopropyl)carbazate >t-Butyl 2-isopropylhydrazinecarboxylate;tert-Butyl 3-(Isopropyl)carbazate;1-tert-Butoxycarbonyl-2-isopropylhydrazine;tert-Butyl 2-isopropylhydrazinecarboxylate;3-(Isopropyl)carbazic Acid tert-Butyl Ester;tert-butyl2-isopropylhydrazine-1-carboxylate;2-Isopropylhydrazinecarboxylic acid tert-butyl ester
- CBNumber
- CB12533921
- Molecular Formula
- C8H18N2O2
- Formula Weight
- 174.24
- MOL File
- 16689-35-3.mol
1-Boc-2-isopropylhydrazine Property
- Melting point:
- 47-51℃
- Boiling point:
- 80°C/0.6mmHg(lit.)
- Density
- 0.956
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- solubility
- soluble in Methanol
- form
- powder to crystal
- color
- White to Almost white
- CAS DataBase Reference
- 16689-35-3
Safety
- HS Code
- 2928009090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H312Harmful in contact with skin
H315Causes skin irritation
H319Causes serious eye irritation
H332Harmful if inhaled
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P312Call a POISON CENTER or doctor/physician if you feel unwell.
P321Specific treatment (see … on this label).
P322Specific measures (see …on this label).
P330Rinse mouth.
P332+P313IF SKIN irritation occurs: Get medical advice/attention.
P362Take off contaminated clothing and wash before reuse.
P363Wash contaminated clothing before reuse.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- B4375
- Product name
- tert-Butyl 3-(Isopropyl)carbazate
- Purity
- >98.0%(GC)(T)
- Packaging
- 1g
- Price
- $54
- Updated
- 2025/07/31
- Product number
- B4375
- Product name
- tert-Butyl 3-(Isopropyl)carbazate
- Purity
- >98.0%(GC)(T)
- Packaging
- 5g
- Price
- $184
- Updated
- 2024/03/01
- Product number
- B694620
- Product name
- tert-Butyl2-Isopropylhydrazinecarboxylate
- Packaging
- 50mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- FB140025
- Product name
- tert-Butyl 2-isopropylhydrazinecarboxylate
- Packaging
- 1g
- Price
- $40
- Updated
- 2021/12/16
- Product number
- AK-83246
- Product name
- tert-Butyl2-isopropylhydrazinecarboxylate
- Purity
- 95%
- Packaging
- 250mg
- Price
- $11
- Updated
- 2021/12/16
1-Boc-2-isopropylhydrazine Chemical Properties,Usage,Production
Synthesis
16689-34-2
16689-35-3
General procedure for the synthesis of 1-Boc-2-isopropylhydrazine from tert-butyl 2-(propan-2-ylidene)hydrazinecarboxylate: tert-butyl 2-(propan-2-ylidene)hydrazinecarboxylate (0.51 g, 3.0 mmol) was dissolved in 20 mL of tetrahydrofuran (THF), sodium cyanoborohydride (NaBH3CN, 0.19 g, 3.0 mmol) and a small amount of bromocresol green was added as the indicator. Subsequently, 1.5 mL of THF solution of p-toluenesulfonic acid (0.57 g, 3.0 mmol) was added slowly and dropwise over about 1 hour, maintaining the pH of the reaction system between 3.5 and 5.0. The reaction mixture was continued to be stirred at room temperature for 1 h before the solvent was removed by rotary evaporation. The residue was extracted by partitioning with ethyl acetate (30 mL) and saturated saline. The organic phase was washed sequentially with saturated sodium bicarbonate solution (20 mL) and saturated saline, and then evaporated to dryness. The obtained residue was dissolved in 10 mL of ethanol, 3.6 mL of 1M sodium hydroxide solution (3.6 mmol) was added and stirred at room temperature for 30 min. After completion of the reaction, the solvent was removed by rotary evaporation and the residue was dissolved in ethyl acetate and extracted with water. The organic layer was evaporated under reduced pressure and the residue was purified by column chromatography to afford tert-butyl 2-isopropylhydrazinecarboxylate (0.4 g, 77% yield) using a dichloromethane solution of 5% methanol as eluent. The product characterization data were as follows: melting point 47-49 °C; thin layer chromatography Rf=0.44 (dichloromethane solution of 5% methanol); 1H NMR (300 MHz, CDCl3) δ 6.03 (s, 1H, NH), 3.92 (s, 1H, NH), 3.14 (m, 1H), 1.46 (s, 9H), 1.02 (d, 6H, J=6 Hz); 13C NMR (300 MHz, CDCl3) δ 157.2, 80.8, 51.2, 28.7, 21.0.
References
[1] Polish Journal of Chemistry, 2002, vol. 76, # 12, p. 1693 - 1697
[2] Journal of the American Chemical Society, 2004, vol. 126, # 21, p. 6759 - 6764
[3] Patent: WO2014/140073, 2014, A1. Location in patent: Page/Page column 24
[4] Chemistry - A European Journal, 2018, vol. 24, # 33, p. 8325 - 8330
[5] Patent: WO2004/56751, 2004, A1. Location in patent: Page 18-19
1-Boc-2-isopropylhydrazine Preparation Products And Raw materials
Raw materials
Preparation Products
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