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Carbamic acid, [(1S)-1-(hydroxymethyl)-3-butynyl]-, 1,1-dimethylethyl ester is a chemical compound with the molecular formula C10H17NO3. It is a derivative of carbamic acid, characterized by its clear, colorless liquid appearance and a slightly sweet odor. Classified as a toxic substance, Carbamic acid, [(1S)-1-(hydroxymethyl)-3-butynyl]-, 1,1-dimethylethyl ester requires careful handling and is commonly used as a pesticide and insecticide.

763122-73-2

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763122-73-2 Usage

Uses

Used in Agricultural Industry:
Carbamic acid, [(1S)-1-(hydroxymethyl)-3-butynyl]-, 1,1-dimethylethyl ester is used as a pesticide for controlling various pests in crops. Its application reason is its ability to inhibit the nervous system in insects, leading to paralysis and eventual death, thus protecting plants from damage.
Used in Industrial Settings:
In industrial applications, Carbamic acid, [(1S)-1-(hydroxymethyl)-3-butynyl]-, 1,1-dimethylethyl ester is used as an insecticide to control insect infestations in various settings. Its effectiveness in disrupting the nervous system of insects makes it a valuable tool for managing insect populations and preventing damage to infrastructure and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 763122-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,3,1,2 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 763122-73:
(8*7)+(7*6)+(6*3)+(5*1)+(4*2)+(3*2)+(2*7)+(1*3)=152
152 % 10 = 2
So 763122-73-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H17NO3/c1-5-6-8(7-12)11-9(13)14-10(2,3)4/h1,8,12H,6-7H2,2-4H3,(H,11,13)/t8-/m0/s1

763122-73-2SDS

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 tert-butyl N-[(2S)-1-hydroxypent-4-yn-2-yl]carbamate

1.2 Other means of identification

Product number -
Other names (2S)-2-tert-butoxycarbonylamino-pent-4-yn-1-ol

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:763122-73-2 SDS

763122-73-2Relevant academic research and scientific papers

2,3,5-Trisubstituted pyridines as selective AKT inhibitors-Part I: Substitution at 2-position of the core pyridine for ROCK1 selectivity

Lin, Hong,Yamashita, Dennis S.,Zeng, Jin,Xie, Ren,Wang, Wenyong,Nidarmarthy, Sirishkumar,Luengo, Juan I.,Rhodes, Nelson,Knick, Victoria B.,Choudhry, Anthony E.,Lai, Zhihong,Minthorn, Elisabeth A.,Strum, Susan L.,Wood, Edgar R.,Elkins, Patricia A.,Concha, Nestor O.,Heerding, Dirk A.

scheme or table, p. 673 - 678 (2010/07/05)

2,3,5-Trisubstituted pyridines have been designed as potent AKT inhibitors that are selective against ROCK1 based on the comparison between AKT and ROCK1 structures. Substitution at the 2-position of the core pyridine is the key element to provide selectivity against ROCK1. An X-ray co-crystal structure of 9p in PKA supports the proposed rationale of ROCK1 selectivity.

INHIBITORS OF AKT ACTIVITY

-

Page/Page column 54; 144, (2010/02/14)

Invented are novel pyridine compounds, the use of such compounds as inhibitors of PKB/AKT kinase activity and in the treatment of cancer and arthritis.

Assembling heterocycle-tethered C-glycosyl and α-amino acid residues via 1,3-dipolar cycloaddition reactions

Dondoni, Alessandro,Giovannini, Pier Paolo,Massi, Alessandro

, p. 2929 - 2932 (2007/10/03)

(Equation Presented) The 1,3-dipolar cycloadditions of C-glycosyl nitrile oxides and acetylenes to an alkyne and an azide, respectively, bearing a masked glycinyl moiety furnished disubstituted isoxazoles and triazoles. Unveiling the glycinyl group in the

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