510-75-8 Usage
Description
Gibberellin A7 is a plant hormone that is isolated from the culture filtrates of the fungus Gibberella fujikuroi. It plays a crucial role in the regulation of plant growth and development by promoting cell elongation and growth.
Uses
Used in Agriculture:
Gibberellin A7 is used as a growth regulator for promoting plant growth and elongation. It helps in increasing the yield and quality of crops by stimulating cell division and elongation, leading to taller and more robust plants.
Used in Plant Tissue Culture:
Gibberellin A7 is used as a growth factor in plant tissue culture to promote the growth and development of plantlets. It aids in the successful propagation of plants by enhancing cell division and elongation, resulting in the formation of healthy and vigorous plantlets.
Used in Seed Germination:
Gibberellin A7 is used as a seed germination promoter to enhance the germination rate and speed up the growth of seedlings. It helps in breaking dormancy and stimulating the growth of the radicle and plumule, leading to faster and more uniform germination.
Used in Fruit Ripening:
Gibberellin A7 is used as a fruit ripening agent to improve the quality and appearance of fruits. It helps in the development of fruit size, color, and texture, making them more appealing and marketable.
Used in Ornamental Plants:
Gibberellin A7 is used as a growth enhancer in ornamental plants to improve their overall appearance and growth. It helps in promoting taller and more robust plants, making them more attractive and desirable for landscaping and decorative purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 510-75-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 510-75:
(5*5)+(4*1)+(3*0)+(2*7)+(1*5)=48
48 % 10 = 8
So 510-75-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H22O5/c1-9-7-18-8-10(9)3-4-11(18)19-6-5-12(20)17(2,16(23)24-19)14(19)13(18)15(21)22/h5-6,10-14,20H,1,3-4,7-8H2,2H3,(H,21,22)/t10-,11-,12+,13-,14-,17?,18+,19-/m1/s1
510-75-8Relevant articles and documents
Novel method for Separation of GA4/GA7 Mixtures
Ku, Yi-Yin,Sawick, David
, p. 801 - 803 (1995)
Preparative separation of GA4 1 and GA7 2 from the commercially available mixture of GA4 1 and GA7 2 was achieved which is predicated upon the discovery of the differential reactivities of GA4 and GA7 toward silyl ether formation and subsequent deprotection. KEYWORDS: Gibberellin acids (GA4 and GA7); separation; selective silylation and desilylation
A New Method for the Deoxygenation of Tertiary and Secondary Alcohols
Dolan, Simon C.,MacMillan, Jake
, p. 1588 - 1589 (2007/10/02)
The derivatisation of alcohols as their methyl oxalyl esters is shown to be a convenient and selective method for deoxygenation by stannyl radicals.
Partial Synthesis of Gibberellin A7 from Gibberellin A3
Beale, Michael H.,MacMillan, Jake
, p. 3536 - 3543 (2007/10/02)
Gibberellin A3 (2) has been converted into gibberellin A7 (1) by the novel reduction of the bridgehead-methanesulphonate (12) by tri-n-butylstannane, followed by hydrolysis of the resulting acetate (14).
