叔丁氧羰基肼

肼基甲酸叔丁酯 | BOC-肼 | 叔-丁基卡唑 | 卡巴酸叔丁酯 | 叔丁基咔唑

1-Boc hydrazine(BOC-NHNH2) | carbazi acid tert-butyl ester | monoBOC-hydrazine | N-[(t-Butyloxy)carbonyl]hydrazine | tert-Butyl carbazate | AS-13557 | iert-butyl carbazate | NSC60250 | teri-butyl carbazate | hydrazinecarboxylic acid tert-butylester | STK0

tert-Butyl carbazate

B106949-10g

10g

≥98%

2-8°C储存,充氩

冰袋运输

对湿度、空气和热敏感

Starting material for the preparation of BOC-azide, a reagent to introduce the BOC amino protection. Reagent for the synthesis of sulfonic and carboxylic hydrazides.用于与乙烯基卤化物进行钯催化交叉偶联反应，生成 N-叔丁氧羰基-N-烯基肼。用于固相多肽合成和 α-氨基醛的光学纯度测定的试剂。可与醛发生缩合反应形成腙，腙可作为合成 HIV-1 蛋白酶抑制剂的中间体。 Starting material for the preparation of BOC-azide, a reagent to introduce the BOC amino protection. Reagent for the synthesis of sulfonic and carboxylic hydrazides. Employed in a palladium-catalyzed cross-coupling with vinyl halides leading to N-Boc-N-alkenylhydrazines. Reagent used in solid phase peptide synthesis and in α-amino aldehyde optical purity determinations. Condenses with aldehydes to form hydrazones which are intermediates in the synthesis of HIV-1 protease inhibitors

870-46-2

C5H12N2O2

132.16 g/mol

1756967

212-795-3

MFCD00007593

70091

CC(C)(C)OC(=O)NN

tert-butyl N-aminocarbamate

1S/C5H12N2O2/c1-5(2,3)9-4(8)7-6/h6H2,1-3H3,(H,7,8)

DKACXUFSLUYRFU-UHFFFAOYSA-N

CC(C)(C)OC(=O)NN

870-46-2

tert-butyl carbazate

Soluble in methanol (100 mg/mL), and ethanol (50 mg/mL).,

37-41°C

2

3

2

132.09 Da

132.09 Da

64.400 Ų

9

0

106

0

1

0.2

1.02

1.427

91 °C

63-65°C

4.1

1756967

60250