Detail of "93779-31-8"

CAS Number:
93779-31-8
Name:
Cyclopenta[b]pyrrole-2-carboxylicacid, octahydro-, phenylmethyl ester, (2S,3aS,6aS)-
Superlist Name:
(S,S,S)-2-Azabicyclo[3,3,0]-octane-carboxylic acid benzylester hydrochloride
Molecular Structure:
Formula:
C₁₅H₂₀ClNO₂
Molecular Weight:
281.78
Deleted CAS:
852546-83-9
Synonyms:
Cyclopenta[b]pyrrole-2-carboxylicacid, octahydro-, phenylmethyl ester, [2S-(2a,3ab,6ab)]-;
Melting Point:
180-182 °C
Boiling Point:
390.5 °C at 760 mmHg
Flash Point:
190 °C
Appearance:
white to light yellow crystal powder

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N-Alkylated dipeptides and their esters: N-Alkylated dipeptides and their esters. Henning, Reiner; Urbach, Hansjoerg (Hoechst A.-G. , Fed. Rep. Ger.). Ger. Offen. DE 3315464 A1 31 Oct 1984, 49 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C07C103-52; C07C143-68; A61K037-02. APPLICATION: DE 83-3315464 28 Apr 1983. DOCUMENT TYPE: Patent CA Section: 34 (Amino Acids, Peptides, and Proteins) Section cross-reference(s): 1, 27 Carboxyalkyl dipeptides R3O2CCHR4NR5COCHR1NHCH(CO2R2)(CH2)nR [I; R = H, (un)substituted C1-8 aliph., C3-9 cycloaliph., C6-12 arom., or C7-14 araliph. residue; R1 = H, (un)substituted cycloaliph., C6-12 arom., or C7-14 araliph.Some chemicals with cas registry numbers like 93779-31-8 are also used. residue, (un)substituted heteroarom. residue with 5-12 ring atoms, or amino acid side chain; R2, R3 = H, (un)substituted C1-6 aliph., C3-9 cycloaliph., C6-12 arom., or C7-16 araliph. residue; CHR4NR5 = C5-15 heterocyclic mono-, bi-, or tricyclic ring system; n = 1, 2] were prepd. by treating R(CH2)nCH(CO2R2)O3SCF3 or R3O2CCHR4NR5COCHR1O3SCF3 with R3O2CCHR4NR5COCHR1NH2 or R(CH2)nCH(CO2R2)NH2, resp. 93779-31-8 which is the cas registry number of one of substances is just one of reagents here. I are useful as antihypertensives (no data) due to their ability to inhibit angiotensin-converting enzyme. Thus, (S,S)-isoquinoline deriv. II was treated with (R)-PhCH2CH2CH(CO2Et)O3SCF3 to give 84% of the (S,S,S)-isomer of title compd. III. ..

N-Alkylated dipeptides and their esters: N-Alkylated dipeptides and their esters. Henning, Reiner; Urbach, Hansjoerg (Hoechst A.-G. , Fed. Rep. Ger.). Ger. Offen. DE 3315464 A1 31 Oct 1984, 49 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C07C103-52; C07C143-68; A61K037-02. APPLICATION: DE 83-3315464 28 Apr 1983. DOCUMENT TYPE: Patent CA Section: 34 (Amino Acids, Peptides, and Proteins) Section cross-reference(s): 1, 27 Carboxyalkyl dipeptides R3O2CCHR4NR5COCHR1NHCH(CO2R2)(CH2)nR [I; R = H, (un)substituted C1-8 aliph., C3-9 cycloaliph., C6-12 arom., or C7-14 araliph. residue; R1 = H, (un)substituted cycloaliph., C6-12 arom., or C7-14 araliph.Some chemicals with cas registry numbers like 93779-31-8 are also used. residue, (un)substituted heteroarom. residue with 5-12 ring atoms, or amino acid side chain; R2, R3 = H, (un)substituted C1-6 aliph., C3-9 cycloaliph., C6-12 arom., or C7-16 araliph. residue; CHR4NR5 = C5-15 heterocyclic mono-, bi-, or tricyclic ring system; n = 1, 2] were prepd. by treating R(CH2)nCH(CO2R2)O3SCF3 or R3O2CCHR4NR5COCHR1O3SCF3 with R3O2CCHR4NR5COCHR1NH2 or R(CH2)nCH(CO2R2)NH2, resp. 93779-31-8 which is the cas registry number of one of substances is just one of reagents here. I are useful as antihypertensives (no data) due to their ability to inhibit angiotensin-converting enzyme. Thus, (S,S)-isoquinoline deriv. II was treated with (R)-PhCH2CH2CH(CO2Et)O3SCF3 to give 84% of the (S,S,S)-isomer of title compd. III. ..