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88559-56-2

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  • (3AR,6AR)-2,2-DIMETHYL-6-[(TRIPHENYLMETHOXY)METHYL]-2H,3AH,4H,6AH-CYCLOPENTA[D][1,3]DIOXOL-4-ONE

    Cas No: 88559-56-2

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88559-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88559-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,5 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88559-56:
(7*8)+(6*8)+(5*5)+(4*5)+(3*9)+(2*5)+(1*6)=192
192 % 10 = 2
So 88559-56-2 is a valid CAS Registry Number.

88559-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3aR,6aR)-2,2-dimethyl-6-[(trityloxy)methyl]-3a,6a-dihydro-4H-cyclopenta[d][1,3]dioxol-4-one

1.2 Other means of identification

Product number -
Other names (3aR,6aR)-2,2-Dimethyl-6-trityloxymethyl-3a,6a-dihydro-cyclopenta[1,3]dioxol-4-one

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88559-56-2 SDS

88559-56-2Upstream product

88559-56-2Relevant articles and documents

Tumor immunity compound and application thereof

-

, (2020/07/14)

Disclosed are a tumor immunity compound and an application thereof. The invention discloses a compound as shown in the formula (I), optical isomers thereof, and pharmaceutically acceptable salts thereof, and an application of the compound as an STING agonist.

Syntheses of cyclopentyl nucleoside (?)-neplanocin A through tetrazole-fragmentation from cyanophosphates

Yoneyama, Hiroki,Uemura, Kenji,Usami, Yoshihide,Harusawa, Shinya

, p. 2143 - 2150 (2018/03/26)

We recently reported a novel synthetic method for five-membered unsaturated cyclic compounds from ketones involving cyanophosphates (CPs) under neutral conditions, in which alkylidene carbenes generated through tetrazole-fragmentation undergo [1,5]-C–H in

Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides

Choi, Won Jun,Moon, Hyung Ryong,Kim, Hea Ok,Ko, Young Mi,Kim, Hye Jin,Lee, Jeong A.,Lee, Kang Man,Yun, Mi Kyung,Shin, Dae Hong,Chun, Moon Woo,Sheen, Yhun Y.,Kim, Kilhyoun,Jeong, Lak Shin

, p. 611 - 613 (2008/02/04)

The preparative and stereoselective synthesis (45-50% overall yields, >50 g scale) of the key carbasugars 7a-d was achieved from D-ribose via stereoselective Grignard reaction and oxidative rearrangement as key reactions. Copyright Taylor & Francis, Inc.

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