(R)-[[(allyloxy)carbonyl]amino](3-chloro-4-hydroxyphenyl)acetic acid

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What is the (R)-[[(allyloxy)carbonyl]amino](3-chloro-4-hydroxyphenyl)acetic acid ?

(R)-[[(allyloxy)carbonyl]amino](3-chloro-4-hydroxyphenyl)acetic acid is , while it's Molecular Formula is C12H12 Cl N O5. Used in Pharmaceutical Industry:
(R)-[[(allyloxy)carbonyl]amino](3-chloro-4-hydroxyphenyl)acetic acid is used as a building block for the synthesis of various drugs and pharmaceutical compounds due to its unique structure and reactivity. Its chiral nature and functional groups make it a versatile component in the development of new pharmaceuticals.
Used in Drug Research and Development:
In the field of drug research and development, (R)-[[(allyloxy)carbonyl]amino](3-chloro-4-hydroxyphenyl)acetic acid serves as a key component for constructing complex molecules with potential therapeutic applications. Its specific reactivity and properties contribute to the exploration of novel drug candidates and the advancement of pharmaceutical research.

What is the CAS number for (R)-[[(allyloxy)carbonyl]amino](3-chloro-4-hydroxyphenyl)acetic acid ?

The CAS number of (R)-[[(allyloxy)carbonyl]amino](3-chloro-4-hydroxyphenyl)acetic acid is 93841-52-2.

More information of (R)-[[(allyloxy)carbonyl]amino](3-chloro-4-hydroxyphenyl)acetic acid 93841-52-2 are:

Synonyms	(R)-[[(allyloxy)carbonyl]amino](3-chloro-4-hydroxyphenyl)acetic acid
CAS?Number	93841-52-2
Molecular Formula	C12H12 Cl N O5
Molecular Weight	285.68038
Density	1.418g/cm3
Boiling Point	470.3°Cat760mmHg
Flash Point	238.2°C
PSA	99.35000
LogP	2.28790

What is (R)-[[(allyloxy)carbonyl]amino](3-chloro-4-hydroxyphenyl)acetic acid (93841-52-2) used for?

(R)-[[(allyloxy)carbonyl]amino](3-chloro-4-hydroxyphenyl)acetic acid is a chiral compound with the molecular formula C13H15ClNO5, derived from 3-chloro-4-hydroxyphenylacetic acid. It is characterized by its unique stereochemistry, denoted by the "(R)" prefix, and features an allyl ester and an amino group in its structure. The presence of a chloro and hydroxy group further enhances its reactivity and properties, making it a valuable building block in the pharmaceutical industry for the synthesis of various drugs and pharmaceutical compounds.

InChI:InChI=1/C12H12ClNO5/c1-2-5-19-12(18)14-10(11(16)17)7-3-4-9(15)8(13)6-7/h2-4,6,10,15H,1,5H2,(H,14,18)(H,16,17)

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