1-N-Boc-2-Methylhydrazine

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Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:1-(t-butyloxy)carbonyl-2-Methylhydrazine
CAS:127799-54-6
Purity:NLT 98% Package:1G;1KG;100KG
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Products Intro: Product Name:1-N-Boc-2-Methylhydrazine
CAS:127799-54-6
Purity:0.98 Package:1KG;10KG;50KG
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Products Intro: Product Name:tert-butyl 2-methylhydrazine-1-carboxylate
CAS:127799-54-6
Purity:98% Package:5KG;1KG
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Products Intro: Product Name:1-Boc-2-methylhydrazine
CAS:127799-54-6
Purity:>=97% Package:0.1g;0.25g;1g;5g;10g;25g;100g
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Products Intro: Product Name:1-N-Boc-2-Methylhydrazine
CAS:127799-54-6
Purity:99% Package:1KG;1USD

1-N-Boc-2-Methylhydrazine manufacturers

1-N-Boc-2-Methylhydrazine Basic information
Product Name:1-N-Boc-2-Methylhydrazine
Synonyms:1-N-Boc-2-Methylhydrazine;1-(t-butyloxy)carbonyl-2-Methylhydrazine;Hydrazinecarboxylic acid, 2-Methyl-, 1,1-diMethylethyl ester;1-(t-butylo×y)carbonyl-2-Methylhydrazine;2-Methylhydrazinecarboxylic acid tert-butyl est;2-Methylhydrazinecarboxylic acid,1,1-dimethylethyl ester;1-Boc-2-methylhydrazine;N2-BOC-N1-Methylhydrazine
CAS:127799-54-6
MF:C6H14N2O2
MW:146.19
EINECS:
Product Categories:
Mol File:127799-54-6.mol
1-N-Boc-2-Methylhydrazine Structure
1-N-Boc-2-Methylhydrazine Chemical Properties
Melting point 49-51℃
density 0.982±0.06 g/cm3 (20 ºC 760 Torr)
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
pka10.73±0.43(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C6H14N2O2/c1-6(2,3)10-5(9)8-7-4/h7H,1-4H3,(H,8,9)
InChIKeyUZRUVUYVHGPEAP-UHFFFAOYSA-N
SMILESN(C(OC(C)(C)C)=O)NC
Safety Information
HS Code 2928009090
MSDS Information
1-N-Boc-2-Methylhydrazine Usage And Synthesis
Synthesis
1-(benzylo×y)carbonyl-2-(t-butylo×y)carbonyl-1-Methylhydrazine

127799-53-5

1-N-Boc-2-Methylhydrazine

127799-54-6

The general procedure for the synthesis of 1-Boc-2-methylhydrazine from 1-Cbz-2-Boc-1-methylhydrazine is as follows: 24.8 g (70.8 mmol) of 1-benzyl-2-tert-butyl-1-methylhydrazine-1,2-dicarboxylate was dissolved in 500 mL of ethanol at room temperature and standard atmospheric pressure, and 1.24 g of palladium (10% activated charcoal) was added as a catalyst for the hydrogenation reaction. Upon completion of the reaction, the reaction mixture was filtered through diatomaceous earth to remove the catalyst and the filtrate was concentrated and dried under reduced pressure to give the product. The yield was 12.3 g with a purity of 48%, representing 57% of the theoretical yield.

References[1] Journal of the Chemical Society - Perkin Transactions 1, 1997, # 16, p. 2297 - 2311
[2] Journal of the American Chemical Society, 1993, vol. 115, # 20, p. 8898 - 8906
[3] Tetrahedron Letters, 1996, vol. 37, # 2, p. 183 - 186
[4] Patent: US5030724, 1991, A
[5] Patent: US2016/52884, 2016, A1. Location in patent: Paragraph 0599-0600
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