20655-61-2

Basic information

• Product Name: Sulfamic acid, cyclohexyl ester
• CAS NO: 20655-61-2
• Molecular Formula: C6H13NO3S
• Molecular Weight: 179.24
• Mol File: 20655-61-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Sulfamic acid, cyclohexyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Sulfamic acid, cyclohexyl ester(20655-61-2)
• EPA Substance Registry System: Sulfamic acid, cyclohexyl ester(20655-61-2)

Safety Data

• Hazardous Substances Data: 20655-61-2(Hazardous Substances Data)

Upstream product

• 100-88-9 cyclohexylsulfamic acid 
• 78441-82-4 3-{2-[(5-dimethylaminomethyl-furan-2-yl)methylthio]ethylamino}-4-amino-1,2,5-thiadiazole 1-oxide 
• 7778-42-9 sulphamoyl chloride 
• 90-05-1 2-methoxy-phenol 
• 136167-44-7 3-(2-methoxyphenoxy)propan-1-ol 
• 627-18-9 1-bromo-3-propanol 
• 108-93-0 cyclohexanol 

Downstream Products

• 1306748-15-1 cyclohexyl N-(cyclohex-2-en-1-yl)sulfamate 

Relevant articles and documents

Intermolecular amination of allyl alcohols with sulfamates: Effective utilization of mercuric catalyst

Herein, we describe the intermolecular amination of allyl alcohols with sulfamates, which have been underutilized as nitrogen nucleophiles for allylic amination. Methyl sulfamate is a good nucleophile in the presence of mercuric triflate and efficiently generates monoallylation products in excellent yield at room temperature. Furthermore, the solid-supported mercuric catalyst silaphenyl mercuric triflate also showed remarkable catalytic activity for the allylic amination. Intermolecular amination of allyl alcohol with sulfamate as a modifiable nitrogen nucleophile is presented. Mercuric reagents act as highly efficient catalyst for the allylic amination, and the procedure was applied to the preparation of various amine derivatives. In many cases, the reaction can be carried out at room temperature and is applicable to a large range of allylic alcohols to give the monoallylated products in excellent yield. Copyright

Compounds having one or more aminosulfaonyloxy radicals useful as pharmaceuticals

Methods of treating chronic arthritis and osteoporosis which utilize both known and novel compounds which would fall under the general formula:(HO)p--A--[--OS(O) 2 NR 1 R 2 ] zwherein A encompasses a wide range of values including but not limited to aryl, loweralkyl, cycloalkyl, and carbohydrates including sucrose and fructose; p is equal to the number of unreacted hydroxy groups contained on the molecule and may be zero; z is the number of --OS(O) 2 NR 1 R 2 groups and is always at least one; R 1 and R 2 are selected from hydrogen, loweralkyl, carboxy and the like; a novel process for preparing the compounds is provided wherein an appropriate sulfamic acid aryl ester is reacted with a hydroxy substituted A radical which may or may not contain thereon protected carboxyl, amino or hydroxy substituents, in an aprotic solvent containing a tertiary amine base. Pharmaceutical compositions for the treatment of chronic arthritis and osteoporosis are also provided.

INTERMEDIATES FOR PREPARING 3,4-DIAMINO-1,2,5-THIADIAZOLES

Histamine H 2-receptor antagonists of the formula STR1 wherein A, m, Z, n and R 1 are as defined herein, and their nontoxic pharmaceutically acceptable salts, hydrates and solvates are novel anti-ulcer agents which are prepared by ring closure of a substi