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CAS RN: 145013-05-4 | Product Number: B4559
1,3-Bis(tert-butoxycarbonyl)thiourea

Purity: >98.0%(N)
Synonyms:
- 1,3-Di-Boc-thiourea
Product Documents:
Size | Unit Price | Shanghai | Tianjin | Japan* |
---|---|---|---|---|
1G |
¥190.00
|
Contact Us | Contact Us | 15 |
5G |
¥620.00
|
1 | Contact Us | 4 |
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Product Number | B4559 |
Purity / Analysis Method ![]() |
>98.0%(N) |
Molecular Formula / Molecular Weight | C__1__1H__2__0N__2O__4S = 276.35 |
Physical State (20 deg.C) | Solid |
Storage Temperature ![]() |
Room Temperature (Recommended in a cool and dark place, <15°C) |
CAS RN | 145013-05-4 |
Reaxys Registry Number | 5815972 |
PubChem Substance ID | 253660653 |
MDL Number | MFCD03093917 |
Specifications
Appearance | White to Almost white powder to crystal |
Purity(with Total Nitrogen) | min. 98.0 % |
Properties (reference)
Melting Point | 132 °C(dec.) |
GHS
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Transport Information:
Customs Control Conditions (Q) |
Application
A Guanidinylating Reagent without Using Mercury Salts
To a solution of starting amine (1 mmol) in dichloromethane (5 mL) at rt are added 1,3-bis(tert-butoxycarbonyl)thiourea (1.05 mmol) and triethylamine (3 mmol). Under stirring, copper(II) chloride (1.05 mmol) is added and the reaction is stirred at rt until adjudged complete by TLC analysis. The reaction is diluted with EtOAc (30 mL) and filtered through a pad of celite. The filtrate is washed with brine (30 mL) and water (30 mL) and dried using anhydrous MgSO4. Filtration and removal of solvent under reduced pressure yields a residue which is purified by silica gel chromatography using gradient elution (hexane : EtOAc). Removal of solvents under vacuum affords the product.
References
- Copper(II) chloride promoted transformation of amines into guanidines and asymmetrical N,N’-disubstituted guanidines
PubMed Literature
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