Tert-Butyl(1R,2S,5S)-2-azido-5-[(dimethylamino)carbonyl]cyclohexylcarbamate oxalic acid CAS NO.:1353893-22-7

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Tert-Butyl(1R,2S,5S)-2-azido-5-[(dimethylamino)carbonyl]cyclohexylcarbamate oxalic acid CAS NO.:1353893-22-7
Details
CAS: 1353893-22-7
MF: C16H29N3O7
MW: 375.42
EINECS: 1592732-453-0
Category
Other Intermediates
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Description
Tert-Butyl(1R,2S,5S)-2-azido-5-[(dimethylamino)carbonyl]cyclohexylcarbamate oxalic acid
Product Name:
Tert-Butyl(1R,2S,5S)-2-azido-5-[(dimethylamino)carbonyl]cyclohexylcarbamate oxalic acid
Synonyms:
Tert-butyl(1R,2S,5S)-2-amino-5-(dimethylcarbamoyl)cyclohexylcarbamateoxalatehydrate;
Tert-Butyl(1R,2S,5S)-2-azido-5-[(dimethylamino)carbonyl]cyclohexylcarbamateoxalic;
tert-butyl{(1R,2S,5S)-2-amino-5-[(dimethylamino)carbonyl]cyclohexyl}carbamatemonooxalatemonohydrate;
N-[(1R,2S,5S)-2-Amino-5-[(dimethylamino)carbonyl]cyclohexyl]carbamicacid1,1-dimethyletChemicalbookhylesterethanedioatehydrate(1:1:1);
5S)-2-azido-5-[(dimethylamino)carbonyl]cyclohexylcarbamateoxalicacid;
Tert-Butyl(1R,2S,5S)-2-azido-5-[(dimethylamino)carbonyl]cycl...;
1353893-22-7Tert-Butyl(1R,2S,5S)-2-azido-5-[(dimethylamino)carbonyl]cyclohexylcarbamateoxalicacid;
tert-butylN-[(1R,2S,5S)-2-amino-5-(dimethylcarbamoyl)cyclohexyl]carbamateoxalatehydrate
CAS:
1353893-22-7
MF:
C16H29N3O7
MW:
375.42
EINECS:
1592732-453-0
Tert-Butyl(1R,2S,5S)-2-azido-5-[(dimethylamino)carbonyl]cyclohexylcarbamate oxalic acid
Storage temp.
Inert atmosphere,Room Temperature
Solubility
Methanol (slightly soluble), water (slightly soluble)
Form
Solid
Color
White to off-white
Tert-Butyl(1R,2S,5S)-2-azido-5-[(dimethylamino)carbonyl]cyclohexylcarbamate oxalic acidUsage
Uses

N-[(1R,2S,5S)-2-amino-5-[(dimethylamino)carbonyl]cyclohexyl]carbamic acid tert-butyl ester oxalate hydrate is an important precursor or intermediate in the synthesis of the antihistamine and allergy treatment drug ​​Ebastine​​ or its key intermediates. It is commonly used in pharmaceutical synthesis to construct the chiral cyclohexylamine scaffold and control amino group protection. This facilitates the subsequent formation of drug molecules with selective H₁ receptor antagonist activity. It is widely used in the research, development, and production of antiallergic and antihistaminic drugs, playing a significant role in relieving allergy symptoms such as urticaria and allergic rhinitis.

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