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92193-74-3

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92193-74-3 Usage

General Description

N2-acetamido-6-benzyloxypurine, also known as ABP or 6-BAP, is a synthetic cytokinin plant hormone that plays a crucial role in promoting cell division and growth in plants. It is commonly used to stimulate the proliferation of shoot and root cultures in tissue culture systems, as well as to enhance the overall growth and development of various plant species. ABP works by activating specific cellular pathways that regulate cell division and differentiation, leading to increased biomass production and improved quality of plant tissue. Additionally, it has been shown to effectively delay senescence and promote the formation of lateral shoots and roots, making it a valuable tool in plant biotechnology and agricultural research.

Check Digit Verification of cas no

The CAS Registry Mumber 92193-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,9 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92193-74:
(7*9)+(6*2)+(5*1)+(4*9)+(3*3)+(2*7)+(1*4)=143
143 % 10 = 3
So 92193-74-3 is a valid CAS Registry Number.

92193-74-3SDS

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 N-(6-phenylmethoxy-7H-purin-2-yl)acetamide

1.2 Other means of identification

Product number -
Other names 2-Acetamino-6-benzyloxy-purin

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:92193-74-3 SDS

92193-74-3Relevant articles and documents

Rapid Entry into Biologically Relevant α,α-Difluoroalkylphosphonates Bearing Allyl Protection-Deblocking under Ru(II)/(IV)-Catalysis

Panigrahi, Kaushik,Fei, Xiang,Kitamura, Masato,Berkowitz, David B.

supporting information, p. 9846 - 9851 (2019/12/24)

A convenient synthetic route to α,α-difluoroalkylphosphonates is described. Structurally diverse aldehydes are condensed with LiF2CP(O)(OCH2CH-CH2)2. The resultant alcohols are captured as the pentafluorophenyl thionocarbonates and efficiently deoxygenated with HSnBu3, BEt3, and O2, and then smoothly deblocked with CpRu(IV)(π-allyl)quinoline-2-carboxylate (1-2 mol %) in methanol as an allyl cation scavenger. These mild deprotection conditions provide access to free α,α-difluoroalkylphosphonates in nearly quantitative yield. This methodology is used to rapidly construct new bis-α,α-difluoroalkyl phosphonate inhibitors of PTPIB (protein phosphotyrosine phosphatase-1B).

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