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Detail of "3471-31-6"

  • MSDS Download
  • CAS Number:
  • 3471-31-6
  • Name:
  • 1H-Indole-3-aceticacid, 5-methoxy-

  • Superlist Name:
  • 5-Methoxyindole-3-acetic acid
  • Molecular Structure:
  • Formula:
  • C11H11NO3
  • Molecular Weight:
  • 205.23
  • Deleted CAS:
  • 110885-75-1
  • Synonyms:
  • Indole-3-aceticacid, 5-methoxy- (6CI,7CI,8CI);(5-Methoxy-1H-indol-3-yl)acetic acid;2-(5-Methoxy-1H-indol-3-yl)acetic acid;2-(5-Methoxy-3-indolyl)acetic acid;5-Methoxy-1H-indole-3-acetic acid;5-Methoxy-3-indoleacetic acid;5-Methoxy-3-indolylacetic acid;5-Methoxy-IAA;5-Methoxyindoleacetic acid;Methoxyindoleacetic acid;
  • EINECS:
  • 222-438-3
  • Melting Point:
  • 145-148 °C (dec.)(lit.)
  • Solubility:
  • insoluble in water
  • Appearance:
  • Off-white to slightly beige crystalline powder

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CAS No.3471-31-6 5-Methoxyindole-3-acetic acid

5-Methoxyindole-3-Acetic Acid

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CAS No.3471-31-6 5-Methoxyindole-3-acetic acid

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CAS No.3471-31-6 5-Methoxyindole-3-acetic acid

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CAS No.3471-31-6 5-Methoxyindole-3-acetic acid

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CAS No.3471-31-6 5-Methoxyindole-3-acetic acid

Assay:98%

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CAS No.3471-31-6 5-Methoxyindole-3-acetic acid

Assay:98%min  Appearance:Light yellow...  Package:as customers...

F.W.:C11H11NO3 M.W.:205.21 M.P.:146-148℃

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CAS No.3471-31-6 5-Methoxyindole-3-acetic acid

5-Methoxy-3-indoleacetic acid.5-Methoxy-3-indoleacetic acid.98%.we can offer a free sample.We're the professional research & develop company, not a trader.We can give the most competitive price.

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CAS No.3471-31-6 5-Methoxyindole-3-acetic acid

Assay:98%  Appearance:Yellow Powde...  Package:Grams~Kilogr...

Molecular Formula: C11H11NO3 Molecular Weight: 205.21

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CAS No.3471-31-6 5-Methoxyindole-3-acetic acid

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Reference

Derivatives of [3H]serotonin in organ cultures of hamster pineal gland
Derivatives of [3H]serotonin in organ cultures of hamster pineal gland. Craft, Cheryl M.; Reiter, Russel J. (Health Sci. 50-67-9 and 73-31-4 are also occured in this study. Cent., Univ. Texas, San Antonio, TX 78284, USA). Life Sci., 34(18), 1775-82 (English) 1984. CODEN: LIFSAK. ISSN: 0024-3205. DOCUMENT TYPE: Journal CA Section: 2 (Mammalian Hormones) Elevated levels of melatonin [73-31-4] (7-fold), 5-hydroxytryptophol [154-02-9] (5-fold), 5-methoxytryptophol [712-09-4] (1.78-fold), and depressed levels of 5-hydroxyindoleacetic acid [54-16-0] (3.8-fold) and methoxyindoleacetic acid [3471-31-6] (1.78-fold) were detected in following the addn. of norepinephrine (NE) [51-41-2] to the medium. In a sep. expt., the melatonin concn. in the media was also periodically measured by RIAto det. the viability of the organ culture over 4 days. The melatonin level on day 2 (2321 pg/gland) was higher than on day 3 (1542 pg/gland) or day 4 (805 pg/gland). The results verify the viability of the hamster pineal organ culture and show that the gland responds to NE in vitro. .
Reciprocal day/night relationship between serotonin oxidation and N-acetylation products in the rat pineal gland
Reciprocal day/night relationship between serotonin oxidation and N-acetylation products in the rat pineal gland. Mefford, Ivan N.; Chang, Peter; Klein, David C.; Namboodiri, M. A. A.; Sugden, David; Barchas, Jack (Sch. Med., Stanford Univ., Stanford, CA 94305, USA). Endocrinology (Baltimore), 113(5), 1582-6 (English) 1983. CODEN: ENDOAO. ISSN: 0013-7227. DOCUMENT TYPE: Journal CA Section: 2 (Mammalian Hormones) Pineal tryptophan [73-22-3], serotonin (5-HT) [50-67-9], N-acetylserotonin [1210-83-9], melatonin [73-31-4], 5-hydroxyindoleacetic acid (5-HIAA) [54-16-0], 5-hydroxytryptophol [154-02-9], 5-methoxytryptophol [712-09-4], and 5-methoxyindoleacetic acid [3471-31-6] were measured by an improved high-pressure liq. chromatog. method with electrochem. detection. 154-02-9 and 9027-33-2 which are cas registry numbers are also used here. The improvements consisted of using MeCN instead of MeOH in the eluant, a slightly higher pH (5.1), and a more efficient reverse-phase column (Ultrasphere C18). A complete anal. required less than the equiv. of 2 rat pineal glands. Samples were obtained at 8 time points. A reciprocal physiol. relation was found between oxidn. and N-acetylation products of 5-HT. 5-HT and the oxidn. products 5-HIAA, 5-hydroxytryptophol, 5-methoxytryptophol, and 5-methoxyindoleacetic acid decreased at night, when the N-acetylation products N-acetylserotonin and melatonin increased. These observations are consistent with the hypothesis that circadian changes in the N-acetylation of 5-HT by indoleamine N-acetyltransferase [9027-33-2] is the major factor controlling circadian changes in the amts. of 5-HT, and 5-HT oxidn. and N-acetylation products in the rat pineal gland. .
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