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Chemical Structure| 1135-40-6 Chemical Structure| 1135-40-6
Chemical Structure| 1135-40-6

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CAPS (Cyclohexylaminopropanesulfonic acid) is a surfactant and dialysis buffer (0.05 M, pH 11).

Synonyms: N-Cyclohexyl-3-aminopropanesulfonic acid

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Product Details of CAPS

CAS No. :1135-40-6
Formula : C9H19NO3S
M.W : 221.32
SMILES Code : OS(=O)(=O)CCCNC1CCCCC1
Synonyms :
N-Cyclohexyl-3-aminopropanesulfonic acid
MDL No. :MFCD00003837
InChI Key :PJWWRFATQTVXHA-UHFFFAOYSA-N
Pubchem ID :70815

Safety of CAPS

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of CAPS

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1135-40-6 ]

[ 1135-40-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1135-40-6 ]
  • [ 51631-50-6 ]
  • [ 39515-51-0 ]
  • [ 51630-58-1 ]
YieldReaction ConditionsOperation in experiment
In n-heptane; water; EXAMPLE 2 Preparation of α-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methyl butanoate using 3-(cyclohexylamino)-propanesulfonic acid as the rate-promoting agent A flask was charged with 3-(cyclohexylamino)propanesulfonic acid (42 mg), 3-phenoxybenzaldehyde (1.90 g, 9.6 mmole), sodium cyanide (0.56 g, 12 mmole), 1 ml water, and 15 ml n-heptane. 2-(4-Chlorophenyl)-3-methylbutanoyl chloride (2.34 g, 10.1 mmole) in 5 ml n-heptane was added dropwise over a period of 24 minutes to the stirred mixture. Thirty minutes after the addition was complete, a total of 54 minutes, glpc indicated a 95.6% yield of the desired ester. After stirring overnight, the reaction mixture was filtered and extracted with ether. The ether was evaporated from the extract, affording α-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methyl butanoate (3.47 g).
In n-heptane; water; EXAMPLE 2 Preparation of α-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methyl butanoate using 3-(cyclohexylamino)propanesulfonic acid as the rate-promoting agent A flask was charged with 3-(cyclohexylamino)propanesulfonic acid (42 mg), 3-phenoxybenzaldehyde (1.90 g, 9.6 mmole), sodium cyanide (0.56 g, 12 mmole), 1 ml water, and 15 ml n-heptane. 2-(4-Chlorophenyl)-3-methylbutanoyl chloride (2.34 g, 10.1 mmole) in 5 ml n-heptane was added dropwise over a period of 24 minutes to the stirred mixture. Thirty minutes after the addition was complete, a total of 54 minutes, glpc indicated a 95.6% yield of the desired ester. After stirring overnight, the reaction mixture was filtered and extracted with ether. The ether was evaporated from the extract, affording α-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methyl butanoate (3.47 g).
 

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