Cas 127758-67-2,(5Z,9E,14Z)-(8S,11R,12S)-11-[(R)-2-((R)-4-Amino-4-carboxy-butyrylamino)-2-(carboxymethyl-carbamoyl)-ethylsulfanyl]-8,12-dihydroxy-icosa-5,9,14-trienoic acid

127758-67-2

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Basic information

Product Name: (5Z,9E,14Z)-(8S,11R,12S)-11-[(R)-2-((R)-4-Amino-4-carboxy-butyrylamino)-2-(carboxymethyl-carbamoyl)-ethylsulfanyl]-8,12-dihydroxy-icosa-5,9,14-trienoic acid
Synonyms:
CAS NO:127758-67-2
Molecular Formula:
Molecular Weight: 643.799
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (5Z,9E,14Z)-(8S,11R,12S)-11-[(R)-2-((R)-4-Amino-4-carboxy-butyrylamino)-2-(carboxymethyl-carbamoyl)-ethylsulfanyl]-8,12-dihydroxy-icosa-5,9,14-trienoic acid(CAS DataBase Reference)
NIST Chemistry Reference: (5Z,9E,14Z)-(8S,11R,12S)-11-[(R)-2-((R)-4-Amino-4-carboxy-butyrylamino)-2-(carboxymethyl-carbamoyl)-ethylsulfanyl]-8,12-dihydroxy-icosa-5,9,14-trienoic acid(127758-67-2)
EPA Substance Registry System: (5Z,9E,14Z)-(8S,11R,12S)-11-[(R)-2-((R)-4-Amino-4-carboxy-butyrylamino)-2-(carboxymethyl-carbamoyl)-ethylsulfanyl]-8,12-dihydroxy-icosa-5,9,14-trienoic acid(127758-67-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 127758-67-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127758-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,5 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 127758-67:
(8*1)+(7*2)+(6*7)+(5*7)+(4*5)+(3*8)+(2*6)+(1*7)=162
162 % 10 = 2
So 127758-67-2 is a valid CAS Registry Number.

127758-67-2Upstream product

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127758-67-2Relevant academic research and scientific papers

(8-R)- and (8-S)-hepoxilin A3. Assignment of configuration and conversion to biologically active conjugates with glutatione

Corey,Su

, p. 2113 - 2116 (1990)

The determination of absolute configuration of (8-R)-hepoxilin A3 (2) (more polar methyl ester) and (8-S)-hepoxilin A3 (3) (less polar methyl ester) is reported along with the synthesis of the biologically active 11-R glutathione thiol conjugates 4 and 5 which may function as important neuromodulators.

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