Acetylheliosupine

Acetylheliosupine

Inquiry
Catalog Number ACM31514304
CAS Number 31514-30-4
Structure
Synonyms 2-Butenoic acid, 2-methyl-, (1S,7aR)-7-[[(2S)-2-[(1S)-1-(acetyloxy)ethyl]-2,3-dihydroxy-3-methyl-1-oxobutoxy]methyl]-2,3,5,7a-tetrahydro-1H-pyrrolizin-1-yl ester, (2Z)- (9CI)
Molecular Weight 439.5
InChI InChI=1S/C22H33NO8/c1-7-13(2)19(25)31-17-9-11-23-10-8-16(18(17)23)12-29-20(26)22(28,21(5,6)27)14(3)30-15(4)24/h7-8,14,17-18,27-28H,9-12H2,1-6H3/b13-7-/t14-,17-,18-,22+/m0/s1
InChI Key LHYJPODIMQKZHJ-ZUFLKMKTSA-N
Purity 95%+
Complexity 786
Covalently-Bonded Unit Count 1
Defined Atom Stereocenter Count 4
Exact Mass 439.22061701
Heavy Atom Count 31
Hydrogen Bond Acceptor Count 9
Hydrogen Bond Donor Count 2
Isomeric SMILES C/C=C(/C)\C(=O)O[C@H]1CCN2[C@H]1C(=CC2)COC(=O)[C@]([C@H](C)OC(=O)C)(C(C)(C)O)O
Monoisotopic Mass 439.22061701
PhysicalState Powder
Rotatable Bond Count 11
Topological Polar Surface Area 123 Ų
Custom Q&A

What is the product name of the chemical compound with CAS number 31514-30-4?

The product name is Acetylheliosupine.

What are some synonyms for Acetylheliosupine?

Some synonyms include 2-Butenoic acid, 2-methyl-, (1S,7aR)-7-[[(2S)-2-[(1S)-1-(acetyloxy)ethyl]-2,3-dihydroxy-3-methyl-1-oxobutoxy]methyl]-2,3,5,7a-tetrahydro-1H-pyrrolizin-1-yl ester, (2Z)- (9CI).

What is the CAS number for Acetylheliosupine?

The CAS number is 31514-30-4.

What is the molecular formula of Acetylheliosupine?

The molecular formula is C22H33NO8.

What is the molecular weight of Acetylheliosupine?

The molecular weight is 439.5.

What is the chemical structure of Acetylheliosupine?

The chemical structure of Acetylheliosupine is (2Z)-C22H33NO8.

What are some potential uses of Acetylheliosupine?

Acetylheliosupine may be used in pharmaceutical research or as a reference in chemical analysis.

Is Acetylheliosupine a natural compound?

Acetylheliosupine is a semi-synthetic compound derived from natural sources.

How is Acetylheliosupine typically synthesized?

Acetylheliosupine is typically synthesized by acetylating and modifying a natural compound to produce the desired structure.

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