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98105-42-1

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98105-42-1 Usage

General Description

TERT-BUTYL [(1S)-2-CYCLOHEXYL-1-FORMYLETHYL]CARBAMATE is a chemical compound that belongs to the carbamate family. It is a white solid that is mainly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. TERT-BUTYL [(1S)-2-CYCLOHEXYL-1-FORMYLETHYL]CARBAMATE is known for its ability to act as a protecting group for amines in organic synthesis. It is also used in the production of various esters and amides. TERT-BUTYL [(1S)-2-CYCLOHEXYL-1-FORMYLETHYL]CARBAMATE is considered to be of low toxicity, and its use is regulated to prevent adverse health and environmental effects.

Check Digit Verification of cas no

The CAS Registry Mumber 98105-42-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,1,0 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98105-42:
(7*9)+(6*8)+(5*1)+(4*0)+(3*5)+(2*4)+(1*2)=141
141 % 10 = 1
So 98105-42-1 is a valid CAS Registry Number.

98105-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Carbamic acid, N-[(1S)-2-cyclohexyl-1-formylethyl]-, 1,1-dimethylethyl ester

1.2 Other means of identification

Product number -
Other names (S)-TERT-BUTYL 1-CYCLOHEXYL-3-OXOPROPAN-2-YLCARBAMATE

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:98105-42-1 SDS

98105-42-1Relevant articles and documents

Immunoregulator

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Paragraph 0119; 0126-0128, (2021/11/26)

The invention discloses an immune regulator, in particular to a compound for inhibiting IL - 17A and application of the compound as an immunomodulator in preparation of medicines. The invention discloses a compound shown in formula I. The application of t

Structure-based design of β1i or β5i specific inhibitors of human immunoproteasomes

De Bruin, Gerjan,Huber, Eva M.,Xin, Bo-Tao,Van Rooden, Eva J.,Al-Ayed, Karol,Kim, Kyung-Bo,Kisselev, Alexei F.,Driessen, Christoph,Van Der Stelt, Mario,Van Der Marel, Gijsbert A.,Groll, Michael,Overkleeft, Herman S.

supporting information, p. 6197 - 6209 (2014/08/18)

Mammalian genomes encode seven catalytic proteasome subunits, namely, β1c, β2c, β5c (assembled into constitutive 20S proteasome core particles), β1i, β2i, β5i (incorporated into immunoproteasomes), and the thymoproteasome-specific subunit β5t. Extensive r

A direct and efficient stereoconservative procedure for the selective oxidation of N-protected β-amino alcohols

Ocejo, Marta,Vicario, Jose L.,Badía, Dolores,Carrillo, Luisa,Reyes, Efraim

, p. 2110 - 2112 (2007/10/03)

An efficient, very simple and eco-friendly procedure has been developed for the synthesis of highly enantioenriched α-amino aldehydes by IBX-mediated oxidation of the corresponding β-amino alcohols. The procedure has been applied to a wide range of substr

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