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Argyrophilic acid, also known as silver-loving acid, is a chemical compound that exhibits a strong affinity for silver ions. It is commonly used in histology and cytology to visualize the distribution of nucleolar organizer regions (NORs) within cells, as these regions are rich in ribosomal RNA genes and silver-staining techniques can highlight them. The argyrophilic reaction involves the use of silver salts, which bind to specific cellular components, producing a visible black or brown coloration under a microscope. This staining method is particularly useful for studying the structure and function of the nucleolus, as well as for diagnostic purposes in various medical fields, such as cancer research and pathology.

20316-84-1

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20316-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20316-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,1 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20316-84:
(7*2)+(6*0)+(5*3)+(4*1)+(3*6)+(2*8)+(1*4)=71
71 % 10 = 1
So 20316-84-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H30O2/c1-13-11-20-10-7-15-18(2,16(20)6-5-14(13)12-20)8-4-9-19(15,3)17(21)22/h14-16H,1,4-12H2,2-3H3,(H,21,22)/t14?,15-,16-,18+,19-,20+/m0/s1

20316-84-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Isocunabic acid

1.2 Other means of identification

Product number -
Other names (-)-Kaurnenoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:20316-84-1 SDS

20316-84-1Relevant articles and documents

BIOSYNTHESIS OF GIBBERELLIN A12-ALDEHYDE, GIBBERELLIN A12 AND THEIR KAURENOID PRECURSORS FROM MEVALONIC ACID IN A CELL-FREE SYSTEM FROM IMMATURE SEED OF PHASEOLUS COCCINEUS

Turnbull, Colin G. N.,Crozier, Alan,Schwenen, Ludger,Graebe, Jan E.

, p. 97 - 102 (2007/10/02)

A cell-free system capable of gibberellin (GA) biosynthesis has been prepared from immature seed of Phaseolus coccineus.This system converted mevalonic acid (MVA) to ent-kaurene, ent-kaurenoic acid, ent-kauradienoic acid, ent-7α-hydroxykaurenoic acid, ent-6α,7α-dihydroxykaurenoic acid, GA12-aldehyde and GA12. ent-Kaurene was converted to ent-kaurenol, ent-kaurenal, ent-kaurenoic acid and ent-7α-hydroxykaurenoic acid.All identifications were by GC/MC.The pathway from MVA to GA12-aldehyde in this species thus appears to be the same as that found in cell-free preparations derived from immature seed of other species.Key Word Index-Phaseolus coccineus; Leguminosae; runner bean; seed development; biosynthesis; cell-free system; HPLC; GC/MC; gibberellin.

KAURENOLIDE BIOSYNTHESIS IN A CELL-FREE SYSTEM FROM CUCURBITA MAXIMA SEEDS

Hedden, Peter,Graebe, Jan E.

, p. 1011 - 1016 (2007/10/02)

A new product obtained by incubation of -mevalonic acid with a cell-free system from Cucurbita maxima endosperm was identified by GC-MS as ent-kaura-6,16-dien-19-oic acid.When this compound was reincubated with the microsomal fraction it was converted to 7β-hydroxykaurenolide and hence to 7β,12α-dihydroxykaurenolide.The dienoic acid was also obtained by incubation of ent-kaurene, ent-kaurenol, ent-kaurenal and ent-kaurenoic acid, but not ent-7α-hydroxykaurenoic acid, with the microsomal fraction.Thus, in the C. maxima cell-free system, the kaurenolides are formed by a pathway which branches from the GA pathway at ent-kaurenoic acid and proceeds via the dienoic acid.Key Word Index- Cucurbita maxima; Cucurbitaceae; biosynthesis; cell-free system; kaurenolides; gibberellins; ent-kaura-6,16-dien-19-oic acid.

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