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BERRYFLOR is a specialized chemical compound designed for use in the agricultural industry, specifically as a foliar fertilizer for berry crops. It is formulated with a micronutrient blend that includes calcium, magnesium, and boron, which are essential for the growth and development of strong and healthy berry plants. BERRYFLOR also contains a balance of trace elements and organic acids to optimize nutrient absorption and promote robust fruit production. BERRYFLOR is known for enhancing overall plant health, improving fruit quality, and increasing yields, making it a popular choice among berry farmers and growers seeking to maximize their crop output.

104986-28-9

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104986-28-9 Usage

Uses

Used in Agricultural Industry:
BERRYFLOR is used as a foliar fertilizer for enhancing the growth and development of berry crops such as strawberries, raspberries, and blueberries. It provides a micronutrient blend of calcium, magnesium, and boron, which are crucial for the health and productivity of these plants.
BERRYFLOR is used as a nutrient optimizer for improving nutrient absorption in berry plants. The balance of trace elements and organic acids in the compound helps to ensure that the plants receive the necessary nutrients for optimal growth and fruit production.
BERRYFLOR is used to enhance overall plant health, contributing to the robustness and resilience of berry plants. This leads to improved resistance against diseases and pests, ultimately resulting in healthier plants.
BERRYFLOR is used to improve fruit quality in berry crops. BERRYFLOR's formulation supports the development of high-quality fruits that are more appealing to consumers and potentially command better market prices.
BERRYFLOR is used to increase yields in berry farming. By promoting robust fruit production and overall plant health, BERRYFLOR helps farmers and growers to achieve higher crop outputs, which can translate to greater profitability and sustainability in their farming operations.

Check Digit Verification of cas no

The CAS Registry Mumber 104986-28-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,9,8 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 104986-28:
(8*1)+(7*0)+(6*4)+(5*9)+(4*8)+(3*6)+(2*2)+(1*8)=139
139 % 10 = 9
So 104986-28-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O4/c1-3-13-10(12)7-5-4-6-8-14-9(2)11/h3-8H2,1-2H3

104986-28-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 6-acetyloxyhexanoate

1.2 Other means of identification

Product number -
Other names Ethyl 6-acetoxyhexanoate

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:104986-28-9 SDS

104986-28-9Downstream Products

104986-28-9Relevant academic research and scientific papers

A lewis acid-promoted pinner reaction

Pfaff, Dominik,Nemecek, Gregor,Podlech, Joachim

supporting information, p. 1572 - 1577 (2013/10/22)

Carbonitriles and alcohols react in a Lewis acid-promoted Pinner reaction to carboxylic esters. Best results are obtained with two equivalents of trimethylsilyl triflate as Lewis acid. Good yields are achieved with primary alcohols and aliphatic or benzylic carbonitriles, but the straightforward synthesis of acrylates and benzoates starting with acrylonitrile and benzonitrile, respectively, is similarly possible. Phenols are not acylated under these reaction conditions. The method has been used for the first total synthesis of the natural product monaspilosin. In the reaction of benzyl alcohols variable amounts of amides are formed in a Ritter-type side reaction.

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