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CAS RN: 107819-90-9 | Product Number: B4535
N,N'-Bis(tert-butoxycarbonyl)-S-methylisothiourea
Purity: >98.0%(HPLC)(N)
Synonyms:
- N,N'-Di-Boc-S-methylisothiourea
- Methyl N,N'-Bis(tert-butoxycarbonyl)carbamimidothioate
- N,N'-Bis(tert-butoxycarbonyl)carbamimidothioic Acid Methyl Ester
- Methyl N,N'-Di-Boc-carbamimidothioate
- N,N'-Di-Boc-carbamimidothioic Acid Methyl Ester
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| Product Number | B4535 |
Purity / Analysis Method
|
>98.0%(HPLC)(N) |
| Molecular Formula / Molecular Weight | C__1__2H__2__2N__2O__4S = 290.38 |
| Physical State (20 deg.C) | Solid |
Storage Temperature
|
Room Temperature (Recommended in a cool and dark place, <15°C) |
| CAS RN | 107819-90-9 |
| Reaxys Registry Number | 5815984 |
| PubChem Substance ID | 253662022 |
| MDL Number | MFCD00239356 |
Specifications
| Appearance | White to Almost white powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Purity(with Total Nitrogen) | min. 98.0 % |
| Melting point | 121.0 to 125.0 °C |
| NMR | confirm to structure |
Properties (reference)
| Melting Point | 123 °C |
GHS
Related Laws:
Transport Information:
| H.S.code* | 2930.90-900 |
Application
A Guanidinylating Reagent

Experimental procedure: To a stirring solution of 1 (272 mg, 0.88 mmol) in anhydrous DMF (10 mL) and N,N'-bis(tert-butoxycarbonyl)-S-methylisothiourea (262 mg, 0.90 mmol) at 0 ℃ is added Et3N (0.37 mL, 2.66 mmol) in one portion, the reaction is stirred for 15 minutes. Then AgNO3 (164 mg, 0.96 mmol) is added, the solution is stirred at 0 ℃ for 3 hours, then room temperature overnight. Filtered the solution through celite, the residue is extracted with water and EtOAc for 3 times. The organic layers are combined and washed with saturated brine, dried over Na2SO4. The crude product is purified by silica gel flash chromatography eluting with 7% EtOAc/hexane to give 2 (455 mg, 86%) as colorless oil.
References
- De Novo Asymmetric Synthesis of (+)-Monanchorin
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